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GB1139138A - Novel derivatives of pentachlorobenzaldehyde - Google Patents

Novel derivatives of pentachlorobenzaldehyde

Info

Publication number
GB1139138A
GB1139138A GB4009066A GB4009066A GB1139138A GB 1139138 A GB1139138 A GB 1139138A GB 4009066 A GB4009066 A GB 4009066A GB 4009066 A GB4009066 A GB 4009066A GB 1139138 A GB1139138 A GB 1139138A
Authority
GB
United Kingdom
Prior art keywords
pentachlorobenzaldehyde
sept
solution
novel derivatives
derivatives
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.)
Expired
Application number
GB4009066A
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.)
Nihon Nohyaku Co Ltd
Original Assignee
Nihon Nohyaku 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 Nihon Nohyaku Co Ltd filed Critical Nihon Nohyaku Co Ltd
Publication of GB1139138A publication Critical patent/GB1139138A/en
Expired legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C255/00—Carboxylic acid nitriles
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
    • C07C205/13—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by hydroxy groups
    • C07C205/26—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by hydroxy groups and being further substituted by halogen atoms

Landscapes

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

Abstract

1,139,138. Pentachlorobenzaldehyde derivatives. NIHON NOHYAKU CO. Ltd. 8 Sept., 1966 [14 Sept., 1965; 15 Sept., 1965], No. 40090/66. Heading C2C. [Also in Division A5] The invention comprises compounds of the general formula in which R is either or -CH=C(CN) 2 . The new compounds may be obtained by reacting pentachlorobenzaldehyde with hydrogen cyanide or malononitrile. Preferably the pentachlorobenzalcyanhydrin is prepared by treating a solution of pentachlorobenzaldehyde with sodium bisulphite solution, adding sodium cyanide solution to the mixture and neutralizing with hydrochloric acid.
GB4009066A 1965-09-14 1966-09-08 Novel derivatives of pentachlorobenzaldehyde Expired GB1139138A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP5587465 1965-09-14
JP5612365 1965-09-15

Publications (1)

Publication Number Publication Date
GB1139138A true GB1139138A (en) 1969-01-08

Family

ID=26396776

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4009066A Expired GB1139138A (en) 1965-09-14 1966-09-08 Novel derivatives of pentachlorobenzaldehyde

Country Status (1)

Country Link
GB (1) GB1139138A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0053321A2 (en) * 1980-11-28 1982-06-09 Bayer Ag Substituted derivatives of phenoxy cinnamic acid, process for their preparation and their use as herbicides

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0053321A2 (en) * 1980-11-28 1982-06-09 Bayer Ag Substituted derivatives of phenoxy cinnamic acid, process for their preparation and their use as herbicides
EP0053321A3 (en) * 1980-11-28 1982-09-22 Bayer Ag Substituted derivatives of phenoxy cinnamic acid, process for their preparation, their use as herbicides, intermediates and the preparation thereof
EP0125506A1 (en) * 1980-11-28 1984-11-21 Bayer Ag 5-(2,6-Dichloro-4-trifluoromethyl-phenoxy)-2-nitrobenzaldehyde-diacetacylal

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