DE3560180D1 - Process for the selective c-alkylation of phenols - Google Patents

Process for the selective c-alkylation of phenols

Info

Publication number
DE3560180D1
DE3560180D1 DE8585400538T DE3560180T DE3560180D1 DE 3560180 D1 DE3560180 D1 DE 3560180D1 DE 8585400538 T DE8585400538 T DE 8585400538T DE 3560180 T DE3560180 T DE 3560180T DE 3560180 D1 DE3560180 D1 DE 3560180D1
Authority
DE
Germany
Prior art keywords
formula
image
optionally
denotes
alkoxycarbonyl
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
DE8585400538T
Other languages
English (en)
Inventor
Gerard Mignani
Didier Morel
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.)
Rhone Poulenc Sante SA
Original Assignee
Rhone Poulenc Sante SA
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 Rhone Poulenc Sante SA filed Critical Rhone Poulenc Sante SA
Application granted granted Critical
Publication of DE3560180D1 publication Critical patent/DE3560180D1/de
Expired legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00—Preparation of carboxylic acid esters
    • C07C67/30—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group
    • C07C67/333—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton
    • C07C67/343—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C213/00—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton
    • C07C213/08—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton by reactions not involving the formation of amino groups, hydroxy groups or etherified or esterified hydroxy groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C37/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring
    • C07C37/11—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by reactions increasing the number of carbon atoms
    • C07C37/14—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by reactions increasing the number of carbon atoms by addition reactions, i.e. reactions involving at least one carbon-to-carbon unsaturated bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C41/00—Preparation of ethers; Preparation of compounds having groups, groups or groups
    • C07C41/01—Preparation of ethers
    • C07C41/18—Preparation of ethers by reactions not forming ether-oxygen bonds
    • C07C41/30—Preparation of ethers by reactions not forming ether-oxygen bonds by increasing the number of carbon atoms, e.g. by oligomerisation

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)
  • Catalysts (AREA)
DE8585400538T 1984-03-22 1985-03-21 Process for the selective c-alkylation of phenols Expired DE3560180D1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR8404443A FR2561641B1 (fr) 1984-03-22 1984-03-22 Procede de c-alcoylation selective des phenols

Publications (1)

Publication Number Publication Date
DE3560180D1 true DE3560180D1 (en) 1987-06-25

Family

ID=9302334

Family Applications (1)

Application Number Title Priority Date Filing Date
DE8585400538T Expired DE3560180D1 (en) 1984-03-22 1985-03-21 Process for the selective c-alkylation of phenols

Country Status (8)

Country Link
US (1) US4594460A (de)
EP (1) EP0161132B1 (de)
JP (1) JPS60215636A (de)
AT (1) ATE27264T1 (de)
CA (1) CA1217779A (de)
DE (1) DE3560180D1 (de)
FR (1) FR2561641B1 (de)
SU (1) SU1480759A3 (de)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0304493B1 (de) * 1987-03-11 1992-09-02 Kanegafuchi Kagaku Kogyo Kabushiki Kaisha Hydroxystyren-derivate
US5089516A (en) * 1987-03-11 1992-02-18 Kanegafuchi Kagaku Kogyo Kabushiki Kaisha 1-phenyl-3,5-pyrazolidinedione hydroxystyrene compounds which have tyrosine kinase inhibiting activity
US5202341A (en) * 1987-03-11 1993-04-13 Kanegafuchi Kagaku Kogyo Kabushiki Kaisha Hydroxystyrene compounds having tyrosine kinase inhibiting activity
DE3725848A1 (de) * 1987-08-04 1989-02-16 Bayer Ag Polymere dihydroxyverbindungen und ihre verwendung als stabilisatoren fuer polymere
US5043510A (en) * 1989-03-27 1991-08-27 E. I. Du Pont De Nemours And Company Aqueous alkylation process
FR2657345B1 (fr) * 1990-01-19 1992-05-07 Rhone Poulenc Chimie Procede de c-alkylation de l'hydroquinone et de ses monoethers.
JP4059531B2 (ja) * 1993-08-18 2008-03-12 エア・ウォーター・ケミカル株式会社 アルコキシナフタレンカルボン酸の製造方法
FR2733977B1 (fr) * 1995-05-10 1997-07-04 Rhone Poulenc Nutrition Animal Procede de preparation de phenols substitues
US20130156708A1 (en) * 2011-12-20 2013-06-20 Symrise Ag Phenol derivatives as antimicrobial agents

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA577711A (en) * 1959-06-16 R. Bader Alfred Method for preparing alkenyl substituted phenolic compounds
CA577710A (en) * 1959-06-16 Pittsburgh Plate Glass Company Method for preparing alkenyl substituted phenolic compounds
US3518318A (en) * 1965-05-14 1970-06-30 Shell Oil Co Octadienyl phenols
JPS53108934A (en) * 1977-03-07 1978-09-22 Eisai Co Ltd 2-methyl-3-prenul-4,5,6-trimethoxy-phenol and its preparation
US4168271A (en) * 1977-04-13 1979-09-18 Scm Corporation Unsaturated vitamin E intermediates--dehydro and didehydro α-tocopherols
JPS56135443A (en) * 1980-03-25 1981-10-22 Sumitomo Chem Co Ltd Preparation of phenol
US4400545A (en) * 1980-10-08 1983-08-23 Fritzsche Dodge & Olcott Inc. Alicyclic ketone and alcohol derivatives

Also Published As

Publication number Publication date
FR2561641A1 (fr) 1985-09-27
US4594460A (en) 1986-06-10
EP0161132A1 (de) 1985-11-13
JPS60215636A (ja) 1985-10-29
FR2561641B1 (fr) 1987-01-09
EP0161132B1 (de) 1987-05-20
CA1217779A (fr) 1987-02-10
SU1480759A3 (ru) 1989-05-15
ATE27264T1 (de) 1987-06-15

Similar Documents

Publication Publication Date Title
DE3560180D1 (en) Process for the selective c-alkylation of phenols
PL333422A1 (en) Method of obtaining benzyl ethers
Komatsu et al. Studies on the constituents of Sophora species. XIII. Constituents of the aerial parts of Sophora tomentosa L.(2)
ES2083685T3 (es) Intermediarios para la sintesis de compuestos de la 19-nor-vitamina d.
IL141316A0 (en) Water soluble prodrugs of hindered alcohols or phenols
MX169001B (es) Mejoras en metodo para preparar un macho y matriz de fundicion
GB2026484B (en) Preparation of phenolic ethers
ISHII et al. Cesium fluoride-mediated Claisen rearrangement of aryl propargyl ether and its application to the synthesis of chelerythrine
CA1192915A (en) Production of hydroquinone
Hutchins et al. Selective reductions of conjugated acetylenes with magnesium in methanol and methanol-D
ES2042979T3 (es) Procedimiento continuo de preparar di alquil carbonatos.
Burke et al. New Synthesis of Trimethylhydroquinone1
KR860001108A (ko) 페닐-나프티리딘의 제조방법
NZ330387A (en) Process for preparing 2-(2-methylphenyl)-3- methoxyacrylic acid methylester by formylating 2-methylphenylacetic acid methylester
Badea et al. Ceric ammonium nitrate in organic synthesis. II. Oxidation of N, N-dimethyl methoxyphenylmethylamines to methoxybenzaldehydes
Maruyama et al. Syntheses of α-and β-lapachones and their homologues by way of photochemical side chain introduction to quinone
Dimmel et al. Pulping catalysts from lignin (7). Nitrogen dioxide oxidation of a lignin model dimer
Mandal et al. A mild and efficient method for selective cleavage of ketals and acetals using lithium chloride in water-dimethyl sulfoxide
ES516349A0 (es) "un procedimiento de preparacion de orto-hidroxibenzaldehidos".
ES2061662T3 (es) Proceso quimico.
ES2028834T3 (es) Metodo para la preparacion de accidos piridin-2,3-dicarboxilico.
Belyanin et al. Efficient procedure for preparing salicyl alcohols
CA2243363A1 (en) Process for producing chromans
FR2750986B1 (fr) Procede de nitration d'un compose phenolique substitue par un groupement electro-attracteur
FR2632951B1 (fr) Procede de preparation de dichloro-2,6 amino-4 phenol

Legal Events

Date Code Title Description
8364 No opposition during term of opposition
8339 Ceased/non-payment of the annual fee