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CN108689856A - A kind of new preparation process of 3- hydroxy-betas-nitrostyrolene - Google Patents

A kind of new preparation process of 3- hydroxy-betas-nitrostyrolene Download PDF

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Publication number
CN108689856A
CN108689856A CN201810741382.1A CN201810741382A CN108689856A CN 108689856 A CN108689856 A CN 108689856A CN 201810741382 A CN201810741382 A CN 201810741382A CN 108689856 A CN108689856 A CN 108689856A
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CN
China
Prior art keywords
hydroxy
nitrostyrolene
betas
added
milligrams
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN201810741382.1A
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Chinese (zh)
Inventor
不公告发明人
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Shanghai Hua Zi Biological Technology Co Ltd
Original Assignee
Shanghai Hua Zi Biological Technology Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Shanghai Hua Zi Biological Technology Co Ltd filed Critical Shanghai Hua Zi Biological Technology Co Ltd
Priority to CN201810741382.1A priority Critical patent/CN108689856A/en
Publication of CN108689856A publication Critical patent/CN108689856A/en
Pending legal-status Critical Current

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C201/00Preparation of esters of nitric or nitrous acid or of compounds containing nitro or nitroso groups bound to a carbon skeleton
    • C07C201/06Preparation of nitro compounds
    • C07C201/12Preparation of nitro compounds by reactions not involving the formation of nitro groups

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

The title of the present invention is a kind of new preparation process of 3- hydroxy-betas-nitrostyrolene.Affiliated technical field is medical science.The technical problems to be solved by the invention are to be related to a kind of new preparation process of more advanced 3- hydroxy-betas-nitrostyrolene.The main points of the technical solution of the technical problems to be solved by the invention are a kind of new preparation methods of the compound.

Description

A kind of new preparation process of 3-hydroxy-betas-nitrostyrolene
Technical field
The present invention relates to pharmaceutical technology fields, specifically, the present invention relates to a kind of the new of 3- hydroxy-betas-nitrostyrolene Preparation method.
Background technology
3- hydroxy-betas-nitrostyrolene is a kind of intermediate feed of important synthesis medical product.
The preparation method yield of existing 3- hydroxy-betas-nitrostyrolene is not high, and synthesis technology is complicated, and yield is unstable, It needs to invent a kind of new preparation method, to overcome the shortcomings of prior art.
Invention content
The present invention uses a kind of new technology, not high for the preparation method yield of existing 3- hydroxy-betas-nitrostyrolene, Synthesis technology is complicated, and yield is unstable, and the disadvantage that the purchase cost of required raw material is high has invented one by long-term research and development The new preparation method of kind has established good technical foundation to overcome the shortcomings of prior art for later industrial production.
The technical scheme is that:
1221 milligrams of 3- hydroxy benzaldehydes are added in the reactor, 30 milliliters of methanol is added, in stirring, is added in room temperature Then 671 milligrams of nitromethane stirs 20 minutes in ice bath, adds 848 milligrams of ammonium acetate, is then stirred at room temperature 4 hours, Reaction solution turns yellow gradually.5 hours are stood, yellow solid is filtered out.It recrystallizes in methyl alcohol again, through filtering, vacuum drying is changed Close object 3- hydroxy-betas-nitrostyrolene, yield 85.6%.
Specific implementation mode
Embodiment 1:The preparation of 3- hydroxy-betas-nitrostyrolene:
1221 milligrams of 3- hydroxy benzaldehydes are added in the reactor, 30 milliliters of methanol is added, in stirring, is added in room temperature Then 671 milligrams of nitromethane stirs 20 minutes in ice bath, adds 848 milligrams of ammonium acetate, is then stirred at room temperature 4 hours, Reaction solution turns yellow gradually.5 hours are stood, yellow solid is filtered out.It recrystallizes in methyl alcohol again, through filtering, vacuum drying is changed Close object 3- hydroxy-betas-nitrostyrolene, yield 85.6%.
Embodiment 2:The preparation of 3- hydroxy-betas-nitrostyrolene:
1221 milligrams of 3- hydroxy benzaldehydes are added in the reactor, 30 milliliters of methanol is added, in stirring, is added in room temperature Then 671 milligrams of nitromethane stirs 20 minutes in ice bath, adds 848 milligrams of ammonium acetate, is then stirred at room temperature 4 hours, Reaction solution turns yellow gradually.5 hours are stood, yellow solid is filtered out.It recrystallizes in methyl alcohol again, through filtering, vacuum drying is changed Close object 3- hydroxy-betas-nitrostyrolene, yield 86.9%.
The present invention can be summarized with others without prejudice to the concrete form of the spirit or essential characteristics of the present invention.Therefore, nothing By from the point of view of which point, the embodiment above of the invention can only all be considered the description of the invention and cannot limit this hair It is bright.

Claims (2)

1. a kind of new preparation process of 3- hydroxy-betas-nitrostyrolene, it is characterized in that:
1221 milligrams of 3- hydroxy benzaldehydes are added in the reactor, 30 milliliters of methanol is added, 671 millis are added in stirring, in room temperature Gram nitromethane, then stirred 20 minutes in ice bath, add 848 milligrams of ammonium acetate, be then stirred at room temperature 4 hours, react Liquid turns yellow gradually.5 hours are stood, yellow solid is filtered out.It recrystallizes in methyl alcohol again, through filtering, vacuum drying obtains compound 3- hydroxy-betas-nitrostyrolene, yield 85.6%.
2. according to the method described in claim 1, it is characterized in that:
It needs that compounds acetic acid ammonium is added in reaction solution.
CN201810741382.1A 2018-07-09 2018-07-09 A kind of new preparation process of 3- hydroxy-betas-nitrostyrolene Pending CN108689856A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201810741382.1A CN108689856A (en) 2018-07-09 2018-07-09 A kind of new preparation process of 3- hydroxy-betas-nitrostyrolene

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201810741382.1A CN108689856A (en) 2018-07-09 2018-07-09 A kind of new preparation process of 3- hydroxy-betas-nitrostyrolene

Publications (1)

Publication Number Publication Date
CN108689856A true CN108689856A (en) 2018-10-23

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
CN201810741382.1A Pending CN108689856A (en) 2018-07-09 2018-07-09 A kind of new preparation process of 3- hydroxy-betas-nitrostyrolene

Country Status (1)

Country Link
CN (1) CN108689856A (en)

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101337898A (en) * 2007-07-06 2009-01-07 南京理工大学 Method for synthesizing m-hydroxyphenylacetamide
WO2011047156A1 (en) * 2009-10-15 2011-04-21 Hercules Technology Management Co V, Inc. Sepiapterin reductase inhibitors for the treatment of pain
CN102348675A (en) * 2009-03-09 2012-02-08 巴斯夫欧洲公司 Process for preparing substituted 2-nitrobiphenyls

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101337898A (en) * 2007-07-06 2009-01-07 南京理工大学 Method for synthesizing m-hydroxyphenylacetamide
CN102348675A (en) * 2009-03-09 2012-02-08 巴斯夫欧洲公司 Process for preparing substituted 2-nitrobiphenyls
WO2011047156A1 (en) * 2009-10-15 2011-04-21 Hercules Technology Management Co V, Inc. Sepiapterin reductase inhibitors for the treatment of pain

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WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20181023

WD01 Invention patent application deemed withdrawn after publication