IE36327L - Production of ketals - Google Patents

Production of ketals

Info

Publication number
IE36327L
IE36327L IE55272A IE55272A IE36327L IE 36327 L IE36327 L IE 36327L IE 55272 A IE55272 A IE 55272A IE 55272 A IE55272 A IE 55272A IE 36327 L IE36327 L IE 36327L
Authority
IE
Ireland
Prior art keywords
formula
benzodioxoles
hydroxy
ion exchange
exchange resin
Prior art date
Application number
IE55272A
Other versions
IE36327B1 (en
Original Assignee
Fisons 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 Fisons Ltd filed Critical Fisons Ltd
Publication of IE36327L publication Critical patent/IE36327L/en
Publication of IE36327B1 publication Critical patent/IE36327B1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C41/00Preparation of ethers; Preparation of compounds having groups, groups or groups
    • C07C41/48Preparation of compounds having groups
    • C07C41/50Preparation of compounds having groups by reactions producing groups
    • C07C41/54Preparation of compounds having groups by reactions producing groups by addition of compounds to unsaturated carbon-to-carbon bonds

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

1386094 Ketals; 4-hydroxy benzodioxoles FISONS Ltd 25 April 1972 [4 May 1971] 12869/71 Heading C2C A process for the preparation of a ketal of the formula wherein R<SP>1</SP> and R<SP>3</SP> are (C 1 -C 4 ) alkyl radicals; R<SP>2</SP> is a (C 1 -C 4 ) primary or secondary alkyl radical and R<SP>4</SP> is a (C 1 -C 4 ) normal alkyl radical, comprises reacting a compound of the formula wherein XH is R<SP>2</SP>, with an alkanol of the formula R<SP>4</SP>OH in the presence of, as catalyst, a strong acid ion exchange resin in the acid form. The reaction is suitably carried in an inert solvent for the starting material, at a temperature of from 10‹ to 60‹ C. using equimolar amounts of the starting materials in the presence of at least 0À1% by weight of the starting material of a sulphonic acid ion exchange resin in the acid form. Examples describe the conversion of 2-methoxy propene to 2,2-dimethoxypropane and the use thereof in the production of 4- hydroxy-benzodioxoles. [GB1386094A]
IE55272A 1971-05-04 1972-04-26 Improvements in or relating to the production of ketals IE36327B1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1286971A GB1386094A (en) 1971-05-04 1971-05-04 Production of ketals

Publications (2)

Publication Number Publication Date
IE36327L true IE36327L (en) 1972-11-04
IE36327B1 IE36327B1 (en) 1976-10-13

Family

ID=10012636

Family Applications (1)

Application Number Title Priority Date Filing Date
IE55272A IE36327B1 (en) 1971-05-04 1972-04-26 Improvements in or relating to the production of ketals

Country Status (2)

Country Link
GB (1) GB1386094A (en)
IE (1) IE36327B1 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112341424B (en) * 2020-11-20 2022-03-18 湖南海利常德农药化工有限公司 Synthesis method of 4-hydroxy-2, 2-dimethyl-1, 3-benzodioxole

Also Published As

Publication number Publication date
GB1386094A (en) 1975-03-05
IE36327B1 (en) 1976-10-13

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