IL26947A - 5-halobenzoic acid derivatives and their preparation - Google Patents
5-halobenzoic acid derivatives and their preparationInfo
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
- C07C205/49—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by carboxyl groups
- C07C205/57—Compounds 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
- C07C205/59—Compounds 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
- C07C205/60—Compounds 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C201/00—Preparation of esters of nitric or nitrous acid or of compounds containing nitro or nitroso groups bound to a carbon skeleton
- C07C201/06—Preparation of nitro compounds
- C07C201/12—Preparation of nitro compounds by reactions not involving the formation of nitro groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C227/00—Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton
- C07C227/14—Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton from compounds containing already amino and carboxyl groups or derivatives thereof
- C07C227/16—Preparation 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C229/00—Compounds containing amino and carboxyl groups bound to the same carbon skeleton
- C07C229/52—Compounds 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
- C07C229/54—Compounds 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
- C07C229/64—Compounds 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
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)
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 |
-
1966
- 1966-11-25 IL IL26947A patent/IL26947A/en unknown
- 1966-11-30 FI FI663184A patent/FI48066C/en active
- 1966-11-30 BE BE690476D patent/BE690476A/xx not_active IP Right Cessation
- 1966-12-02 DE DE1543885A patent/DE1543885C3/en not_active Expired
- 1966-12-06 ES ES0334733A patent/ES334733A1/en not_active Expired
- 1966-12-07 CS CS7793A patent/CS150934B2/cs unknown
- 1966-12-08 FR FR86769A patent/FR1504227A/en not_active Expired
- 1966-12-08 NO NO165905A patent/NO132956C/no unknown
- 1966-12-09 CH CH1762266A patent/CH486415A/en not_active IP Right Cessation
- 1966-12-09 BR BR185258/66A patent/BR6685258D0/en unknown
- 1966-12-10 OA OA52690A patent/OA02685A/en unknown
- 1966-12-12 GB GB55530/66A patent/GB1159938A/en not_active Expired
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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