IES20180086A2 - Drug intermediates isovaleric acid synthesis method - Google Patents

Drug intermediates isovaleric acid synthesis method

Info

Publication number
IES20180086A2
IES20180086A2 IES20180086A IES20180086A IES20180086A2 IE S20180086 A2 IES20180086 A2 IE S20180086A2 IE S20180086 A IES20180086 A IE S20180086A IE S20180086 A IES20180086 A IE S20180086A IE S20180086 A2 IES20180086 A2 IE S20180086A2
Authority
IE
Ireland
Prior art keywords
solution
added
isovaleric acid
mol
synthesis method
Prior art date
Application number
IES20180086A
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 IES20180086A2 publication Critical patent/IES20180086A2/en
Publication of IES86991B2 publication Critical patent/IES86991B2/en

Links

Classifications

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

Landscapes

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

Abstract

Drug intermediates isovaleric acid synthesis method, comprises the following steps: 2 mol 1-chloro-3-isopropylacetone and 4-5 mol dimethyl carbonate solution were added to the reaction vessel, control the stirring speed at 110-140 rpm, the solution temperature was raised to 30-40 t, and then added 3-4 mol manganese chloride, reacted for 70-90 min, added 900 ml potassium chloride solution, reduced the temperature of the solution to 20-25 °C, added potassium hydrogen sulfate solution to adjust the pH to 4-5, standing for 50-70 mm, the solution was layered, washed with a methyl carbitol solution, washed with a methyl hydrazine solution, recrystallized from 1-methylpiazepine solution, and dehydrated with the dehydrating agent, finally obtained the product isovaleric acid.
IES20180086A 2017-04-05 2018-04-03 Drug intermediates isovaleric acid synthesis method IES86991B2 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201710216243.2A CN108238893A (en) 2017-04-05 2017-04-05 A kind of synthetic method of pharmaceutical intermediate isovaleric acid

Publications (2)

Publication Number Publication Date
IES20180086A2 true IES20180086A2 (en) 2019-04-03
IES86991B2 IES86991B2 (en) 2019-05-01

Family

ID=59220686

Family Applications (1)

Application Number Title Priority Date Filing Date
IES20180086A IES86991B2 (en) 2017-04-05 2018-04-03 Drug intermediates isovaleric acid synthesis method

Country Status (4)

Country Link
CN (1) CN108238893A (en)
AU (1) AU2018100421A4 (en)
GB (1) GB201708117D0 (en)
IE (1) IES86991B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110776412B (en) * 2019-11-12 2022-04-22 万华化学集团股份有限公司 Method for preparing isovaleric acid, ligand, complex and application thereof in catalytic system

Also Published As

Publication number Publication date
AU2018100421A4 (en) 2018-05-10
GB201708117D0 (en) 2017-07-05
IES86991B2 (en) 2019-05-01
CN108238893A (en) 2018-07-03

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