IES20180089A2 - Drugs intermediates 2,5-dichlorobenzoic acid synthesis method - Google Patents

Drugs intermediates 2,5-dichlorobenzoic acid synthesis method

Info

Publication number
IES20180089A2
IES20180089A2 IES20180089A IES20180089A IES20180089A2 IE S20180089 A2 IES20180089 A2 IE S20180089A2 IE S20180089 A IES20180089 A IE S20180089A IE S20180089 A IES20180089 A IE S20180089A IE S20180089 A2 IES20180089 A2 IE S20180089A2
Authority
IE
Ireland
Prior art keywords
solution
added
washed
mol
dichlorobenzoic acid
Prior art date
Application number
IES20180089A
Inventor
Yan Yida
Original Assignee
Chengdu Dong Dian Ai Er Tech 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 Chengdu Dong Dian Ai Er Tech Co Ltd filed Critical Chengdu Dong Dian Ai Er Tech Co Ltd
Publication of IES20180089A2 publication Critical patent/IES20180089A2/en
Publication of IES86994B2 publication Critical patent/IES86994B2/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/16Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Drugs intermediates 2,5-dichlorobenzoic acid synthesis method, comprises the following steps: 2 mol 2,5-dichloro-6-aminobenzoic acid, 3-5 mol diisobutyl adipate solution were added to the reaction vessel, the temperature of the solution was raised to 70-78 and the stirring speed was controlled at 130-160 rpm, 3-4 mol cobalt naphthenate was added by 3-5 times, each time the interval was about 30-40 min, continued to react for 90-120 min, added 1200 ml potassium chloride solution, after the solution layered, reduced the solution temperature to 10-15 °C, added oxalic acid solution to adjust the pH to 4-5, washed with potassium sulfate solution, washed with methyl tert-butyl ether solution, and washed with 2-methyl tetrahydrofuran solution, vacuum distillation, collected fractions of 110-120 °C, dehydrated with dehydrating agent, finally obtained 2,5-dichlorobenzoic acid.
IES20180089A 2017-04-05 2018-04-03 Drugs intermediates 2,5-dichlorobenzoic acid synthesis method IES86994B2 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201710218741.0A CN108238900A (en) 2017-04-05 2017-04-05 A kind of synthetic method of pharmaceutical intermediate 2,5- dichlorobenzoic acids

Publications (2)

Publication Number Publication Date
IES20180089A2 true IES20180089A2 (en) 2019-04-03
IES86994B2 IES86994B2 (en) 2019-05-01

Family

ID=59220646

Family Applications (1)

Application Number Title Priority Date Filing Date
IES20180089A IES86994B2 (en) 2017-04-05 2018-04-03 Drugs intermediates 2,5-dichlorobenzoic acid synthesis method

Country Status (4)

Country Link
CN (1) CN108238900A (en)
AU (1) AU2018100423A4 (en)
GB (1) GB201708119D0 (en)
IE (1) IES86994B2 (en)

Also Published As

Publication number Publication date
CN108238900A (en) 2018-07-03
AU2018100423A4 (en) 2018-05-17
IES86994B2 (en) 2019-05-01
GB201708119D0 (en) 2017-07-05

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