GB1143417A - Production of 2,2-dimethylpropanol-(3)-al-(1) - Google Patents

Production of 2,2-dimethylpropanol-(3)-al-(1)

Info

Publication number
GB1143417A
GB1143417A GB2442266A GB2442266A GB1143417A GB 1143417 A GB1143417 A GB 1143417A GB 2442266 A GB2442266 A GB 2442266A GB 2442266 A GB2442266 A GB 2442266A GB 1143417 A GB1143417 A GB 1143417A
Authority
GB
United Kingdom
Prior art keywords
isobutyraldehyde
june
formaldehyde
production
aqueous
Prior art date
Legal status (The legal status 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 status listed.)
Expired
Application number
GB2442266A
Other languages
English (en)
Inventor
Rolf Platz
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BASF SE
Original Assignee
BASF SE
Badische Anilin and Sodafabrik AG
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 BASF SE, Badische Anilin and Sodafabrik AG filed Critical BASF SE
Publication of GB1143417A publication Critical patent/GB1143417A/en
Expired legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/02Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/06Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing polymers
    • B01J31/08Ion-exchange resins
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/61Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
    • C07C45/67Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton
    • C07C45/68Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
    • C07C45/72Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction of compounds containing >C = O groups with the same or other compounds containing >C = O groups
    • C07C45/75Reactions with formaldehyde
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2231/00Catalytic reactions performed with catalysts classified in B01J31/00
    • B01J2231/30Addition reactions at carbon centres, i.e. to either C-C or C-X multiple bonds
    • B01J2231/34Other additions, e.g. Monsanto-type carbonylations, addition to 1,2-C=X or 1,2-C-X triplebonds, additions to 1,4-C=C-C=X or 1,4-C=-C-X triple bonds with X, e.g. O, S, NH/N
    • B01J2231/3411,2-additions, e.g. aldol or Knoevenagel condensations
    • B01J2231/342Aldol type reactions, i.e. nucleophilic addition of C-H acidic compounds, their R3Si- or metal complex analogues, to aldehydes or ketones

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
GB2442266A 1965-06-02 1966-06-01 Production of 2,2-dimethylpropanol-(3)-al-(1) Expired GB1143417A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEB82223A DE1235883B (de) 1965-06-02 1965-06-02 Verfahren zur Herstellung von 2, 2-Dimethyl-propanol-(3)-al-(1)

Publications (1)

Publication Number Publication Date
GB1143417A true GB1143417A (en) 1969-02-19

Family

ID=6981425

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2442266A Expired GB1143417A (en) 1965-06-02 1966-06-01 Production of 2,2-dimethylpropanol-(3)-al-(1)

Country Status (4)

Country Link
BE (1) BE681752A (da)
DE (1) DE1235883B (da)
GB (1) GB1143417A (da)
NL (1) NL6607157A (da)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998029374A1 (en) * 1996-12-30 1998-07-09 Neste Chemicals Oy Process for the preparation of polyvalent alcohols

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1793512C3 (de) * 1968-09-27 1987-05-07 Basf Ag, 6700 Ludwigshafen Verfahren zur Herstellung von 2,2- Dimethyl-3-hydroxypropanal

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998029374A1 (en) * 1996-12-30 1998-07-09 Neste Chemicals Oy Process for the preparation of polyvalent alcohols
US6255541B1 (en) 1996-12-30 2001-07-03 Neste Chemical Oy Process for the preparation of polyvalent alcohols

Also Published As

Publication number Publication date
BE681752A (da) 1966-11-28
NL6607157A (da) 1966-12-05
DE1235883B (de) 1967-03-09

Similar Documents

Publication Publication Date Title
BE695645A (fr) Procede de preparation de resines macroporeuses, et applications de celles-ci a l'obtention d'echangeurs d'ions.
GB1258963A (da)
GB1166961A (en) Process for Producing beta-Methylmercaptopropionaldehyde
GB1143417A (en) Production of 2,2-dimethylpropanol-(3)-al-(1)
GB1222322A (en) Process for the production of vitamin c
GB1318999A (en) Production of 4-ureideohexahydropyrimidin-2-one
GB1348169A (en) Production of hydroxyethyl ethers of butyne-2-diol-1,4
GB1320387A (en) Production of beta-hydroxyaldehydes
GB920759A (en) Method for making methylolacrylamide
SU400706A1 (ru) Способ получения защитного покрытия для фрезерного торфа
GB1233796A (en) pURIFICATION DE 2,2-DIMETHYL-1,3-PROPANDIOL-MONO(HYDROXYPIVALATE)
US1590961A (en) Process for the manufacture of artificial resins
GB1320947A (en) Production of 2,2-dimethyl-1,3-propanediolhydroxypivalic monoester
NL7113286A (en) Drilling fluid additives - based on reaction products of sulphonated lignite or humic acid with phenolic condensates
GB1379444A (en) Continuous production of methylal
GB954533A (en) Process for dehydration of hydroxy carbonyl compounds
NO803861L (no) Fremgangsmaate for fremstilling av blandingskondensater av fenol og melamin
ES447636A1 (es) Metodo de producir 3,5-deterbutil-4-hidroxibenzaldeludo.
GB1132666A (en) Process for the fine purification of oxo-aldehydes
JPS5716877A (en) Production of polyalkyl-2- 2,4-dihydroxyphenyl -7-hydroxy- chroman
GB977283A (en) Process for the preparation of adducts from alcohols and ª‡:ª‰-unsaturated carbonyl compounds
GB987347A (en) Process for purifying acrylonitrile from acetonitrile
GB535408A (en) Preparation of lacquers containing melamine formaldehyde condensation products
GB1235138A (en) Production of formaldehyde solutions
ES389908A1 (es) Procedimiento de produccion de aminas secundarias a partir de animas primarias por condensacion de las mismas con ceto-nas, aldehidos o aril-oxidrilos.