IL26947A - 5-halobenzoic acid derivatives and their preparation - Google Patents

5-halobenzoic acid derivatives and their preparation

Info

Publication number
IL26947A
IL26947A IL26947A IL2694766A IL26947A IL 26947 A IL26947 A IL 26947A IL 26947 A IL26947 A IL 26947A IL 2694766 A IL2694766 A IL 2694766A IL 26947 A IL26947 A IL 26947A
Authority
IL
Israel
Prior art keywords
preparation
acid derivatives
hydrogen
formula
group
Prior art date
Application number
IL26947A
Original Assignee
Ile De France
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 Ile De France filed Critical Ile De France
Publication of IL26947A publication Critical patent/IL26947A/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C205/00Compounds containing nitro groups bound to a carbon skeleton
    • C07C205/49Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by carboxyl groups
    • C07C205/57Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by carboxyl groups having nitro groups and carboxyl groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
    • C07C205/59Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by carboxyl groups having nitro groups and carboxyl groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton the carbon skeleton being further substituted by singly-bound oxygen atoms
    • C07C205/60Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by carboxyl groups having nitro groups and carboxyl groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton the carbon skeleton being further substituted by singly-bound oxygen atoms in ortho-position to the carboxyl group, e.g. nitro-salicylic acids
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C227/00Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C227/14Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton from compounds containing already amino and carboxyl groups or derivatives thereof
    • C07C227/16Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton from compounds containing already amino and carboxyl groups or derivatives thereof by reactions not involving the amino or carboxyl groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C229/00Compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C229/52Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton
    • C07C229/54Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton with amino and carboxyl groups bound to carbon atoms of the same non-condensed six-membered aromatic ring
    • C07C229/64Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton with amino and carboxyl groups bound to carbon atoms of the same non-condensed six-membered aromatic ring the carbon skeleton being further substituted by singly-bound oxygen atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Footwear And Its Accessory, Manufacturing Method And Apparatuses (AREA)

Description

acid derivatives and their preparation DE la present invention provides acid derivatives of the general in which is a or or amino is hydrogen or lower and I a halogen The acid derivatives of formula I according to the are useful as key intermediates for the preparation which possess useful medical activities such as a anesthetic and present invention also provides a process the preparatio acid ester derivatives of formula I in which is which comprises reacting a acid derivative having the general I in is hydrogen with a compound of the general formula which an is hydrogen and is halogen or hydrogen or and together represent the group of alkoxy group referred to hereto are examples of the group are butanamido and pentanamido of the alkyl are and butyl examples of group propylidene and biitylidene radicals and examples of halogen atom are starting materials formula I in which is in thi are novel and some of acid can be pared by reacting in presence of hydrous carbonate carbon dioxide increased pressure in autoclaveψ and acid can prepared by reacting with the others ma be prepared by the same processes as disclosed She compounds are halides or in which some example mono sulfates are mono some examples of halides are methyl ethyl butyl propy and some examples of are In case where mono sulfates or alkyl halides are used starting it is preferable to carry out the reaction in the presence of a basic agent such as metal alkaline earth metal metal alkaline earth metal carbonate fe reactio may be carried out in the presence or of The reaction may be carried out in a will depend on the kind of o are preferably used in mono sulfates are used as the compounds aromatic dimethyl in the cases using and in the cases where are The reaction generally carried out under and reflux in case of using the mono d sulfates halides9 and generally at room temperature in o using the examples will serve to illustrate the 1 fo a solution of g of acid dissolved in ml of absolute g of potassium carbonate anhydride was added with stirring under and further g of dimethyl ture was refluxed with stirring for 15 hours and then filtrate was treated wit active carbon and the solvent was distilled residu was from aqueous methanol to obtain methyl as white yield AnalysisJ Calculated for C I a solution of g benzoic acid dissolved in 100 ml of absolute of potassium ml of dimethyl sulfate and 10 ml of heating at 16 After the reaction was the reaction mixture was filtrated and further residual cakes washed The washings and the filtrate were incorporated and the solvent was distilled off to obtain g of methyl zoate as colorless scaled Yield was crystals were reerystallized from a mixed solvent of 85 ml of methanol and ml of water using of active carbon to obtain g of the purified crystals as colorless yield Calculated for 4 S Found G insufficientOCRQuality

Claims (1)

1. aeid derivatives of the formula in is a hydroxy or is an nitro or amino is hydrogen or lower and X is halogen A process for the preparation of acid ester derivatives of formula I in Claim in which is an alkyl group and is an group wherein a acid derivative having the general formula in in which is is reacted with a compound havin the general in which is an alkylidene is a hydrogen atom and a halogen atom the where is a hydrogen or an alkyl or and together represen the group insufficientOCRQuality
IL26947A 1965-12-10 1966-11-25 5-halobenzoic acid derivatives and their preparation IL26947A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP7613165 1965-12-10

Publications (1)

Publication Number Publication Date
IL26947A true IL26947A (en) 1970-12-24

Family

ID=13596371

Family Applications (1)

Application Number Title Priority Date Filing Date
IL26947A IL26947A (en) 1965-12-10 1966-11-25 5-halobenzoic acid derivatives and their preparation

Country Status (12)

Country Link
BE (1) BE690476A (en)
BR (1) BR6685258D0 (en)
CH (1) CH486415A (en)
CS (1) CS150934B2 (en)
DE (1) DE1543885C3 (en)
ES (1) ES334733A1 (en)
FI (1) FI48066C (en)
FR (1) FR1504227A (en)
GB (1) GB1159938A (en)
IL (1) IL26947A (en)
NO (1) NO132956C (en)
OA (1) OA02685A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102311357B (en) * 2011-10-17 2014-01-08 上海安诺芳胺化学品有限公司 Preparation method of 2-hydroxy-4-aminobenzoic acid

Also Published As

Publication number Publication date
NO132956C (en) 1976-02-11
CH486415A (en) 1970-02-28
DE1543885C3 (en) 1974-02-28
BE690476A (en) 1967-05-30
CS150934B2 (en) 1973-09-17
FI48066C (en) 1974-06-10
FR1504227A (en) 1967-12-01
FI48066B (en) 1974-02-28
NO132956B (en) 1975-11-03
DE1543885A1 (en) 1970-01-02
ES334733A1 (en) 1967-10-16
OA02685A (en) 1970-12-15
BR6685258D0 (en) 1973-12-04
DE1543885B2 (en) 1973-08-02
GB1159938A (en) 1969-07-30

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