IES20180081A2 - Organic synthesis raw materials valeric acid syntesis method - Google Patents

Organic synthesis raw materials valeric acid syntesis method

Info

Publication number
IES20180081A2
IES20180081A2 IES20180081A IES20180081A IES20180081A2 IE S20180081 A2 IES20180081 A2 IE S20180081A2 IE S20180081 A IES20180081 A IE S20180081A IE S20180081 A IES20180081 A IE S20180081A IE S20180081 A2 IES20180081 A2 IE S20180081A2
Authority
IE
Ireland
Prior art keywords
solution
valeric acid
added
raw materials
mol
Prior art date
Application number
IES20180081A
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 IES20180081A2 publication Critical patent/IES20180081A2/en
Publication of IES86975B2 publication Critical patent/IES86975B2/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)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Inorganic Compounds Of Heavy Metals (AREA)

Abstract

Organic synthesis raw materials valeric acid synthesis method, comprises the following steps: 3 mol methyl propyl ketone, 4-6 mol tributyl citrate solution were added to the reaction vessel, controlled the stirring speed at 190-220 rpm, the solution temperature was reduced to 6-9°C for 60-80 min, and then the solution temperature was raised to 10-15 °C, added 3-4 mol chromium acetate by 3-6 times, interval for 30-40 min each time, continued to react for 2-3 h, and then standing for 60-80 min, added 300 ml potassium nitrate solution, standing for solution layer, the water layerextracted with 4-heptanone solution by 3-5 times, extracted with 3-methy1-2- pentanone solution by 4-6 times, combined with the oil layer and extraction, recrystallized in the isobutyl butyrate solution, dehydrated with dehydration, got the finished valeric acid.
IES20180081A 2017-04-05 2018-03-27 Organic synthesis raw materials valeric acid syntesis method IES86975B2 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201710215444.0A CN108238891A (en) 2017-04-05 2017-04-05 A kind of synthetic method of organic synthesis raw material valeric acid

Publications (2)

Publication Number Publication Date
IES20180081A2 true IES20180081A2 (en) 2019-04-03
IES86975B2 IES86975B2 (en) 2019-05-01

Family

ID=59220701

Family Applications (1)

Application Number Title Priority Date Filing Date
IES20180081A IES86975B2 (en) 2017-04-05 2018-03-27 Organic synthesis raw materials valeric acid syntesis method

Country Status (4)

Country Link
CN (1) CN108238891A (en)
AU (1) AU2018100420A4 (en)
GB (1) GB201708116D0 (en)
IE (1) IES86975B2 (en)

Also Published As

Publication number Publication date
GB201708116D0 (en) 2017-07-05
IES86975B2 (en) 2019-05-01
CN108238891A (en) 2018-07-03
AU2018100420A4 (en) 2018-05-10

Similar Documents

Publication Publication Date Title
CA2864676C (en) Methods and kits for reducing non-specific nucleic acid amplification
JP2016513641A5 (en)
MX2016012430A (en) Catalyst assisted hydrothermal conversion of biomass to crude bio-oil.
RU2016115081A (en) METHOD FOR PRODUCING XANTHOGUMOL
BR112017013040A2 (en) method for improving palm oil yields from palm fruit or palm fruit liquid
IES20180081A2 (en) Organic synthesis raw materials valeric acid syntesis method
WO2017024229A8 (en) Stereospecific process for 3-heterocyclylcycloaliphatic-1,2-diols
CN106350618A (en) Making method of breathable and environmentally friendly leather
Madhava Reddy et al. Synthesis of polysubstituted pyrroles in aqueous medium directly from nitro compounds
IES20180089A2 (en) Drugs intermediates 2,5-dichlorobenzoic acid synthesis method
林维臣 et al. Synthesis, crystal structure and characterization of a new zinc citrate complex
IE20180281U1 (en) Benzoyl peroxide organic intermediates synthesis method
IES20180277U1 (en) Organic intermediate 1,6-cyclohexanedione synthesis method
TR201904063T4 (en) Methods for the preparation of ammonium salts of C4 diacids by fermentation and integrated methods for the preparation of their C4 derivatives.
IES20180203A2 (en) Chlormadinone drug intermediates o-tetrachlorobenzoquinone synthesis method
IE20180194U1 (en) Pharmaceutical intermediates androstane-2,3-break-17-ketone-2,3-dicarboxylic acid synthesis method
IES20180276U1 (en) Organic synthesis intermediate 4-methylcyclohexanone synthesis method
IE20180280U1 (en) Methylchloroperoxybenzoic acid drug intermediates synthesis method
IE20180283U1 (en) O-toluene formamide organic intermediates synthesis method
IES20180270U1 (en) Organic analytical reagent diphenylcarbazone synthesis method
IES20180204A2 (en) Organic intermediates oxalic acid aldehydes synthesis method
IE20180282U1 (en) Dodecanoyl peroxide organic intermediates synthesis method
Monastyrskaya SOCIOLOGICAL MONITORING OF MIGRANTS'CHILDREN SOCIOCULTURAL ADAPTATION IN THE EDUCATIONAL ENVIRONMENT
IES20180250A2 (en) Butyraldehyde oxime drug itermediates synthesis method
IES20180117A2 (en) Drug synthesis intermediates p-carboxybenzenesulfonic amide synthesis method