ES506788A0 - Un procedimiento para preparar un fenilacetato de bencilo. - Google Patents

Un procedimiento para preparar un fenilacetato de bencilo.

Info

Publication number: ES506788A0
Authority: ES; Spain
Prior art keywords: sub; sup; alkyl; benzyl; formula
Prior art date: 1980-11-03
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.): Granted

Application number

ES506788A

Other languages

English (en)

Other versions

ES8206431A1 (es

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.)

Eli Lilly and Co

Original Assignee

Eli Lilly and Co

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.)

1980-11-03

Filing date

1981-11-02

Publication date

1982-08-16

1981-11-02 Application filed by Eli Lilly and Co filed Critical Eli Lilly and Co

1982-08-16 Publication of ES506788A0 publication Critical patent/ES506788A0/es

1982-08-16 Publication of ES8206431A1 publication Critical patent/ES8206431A1/es

Status Expired legal-status Critical Current

Links

MIYFJEKZLFWKLZ-UHFFFAOYSA-N Phenylmethyl benzeneacetate Chemical compound C=1C=CC=CC=1COC(=O)CC1=CC=CC=C1 MIYFJEKZLFWKLZ-UHFFFAOYSA-N 0.000 title abstract 2
238000000034 method Methods 0.000 title abstract 2
125000000217 alkyl group Chemical group 0.000 abstract 3
-1 alkali metal phenylacetate Chemical class 0.000 abstract 2
125000003545 alkoxy group Chemical group 0.000 abstract 2
229910052739 hydrogen Inorganic materials 0.000 abstract 2
239000001257 hydrogen Substances 0.000 abstract 2
125000004356 hydroxy functional group Chemical group O* 0.000 abstract 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical group C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 abstract 1
AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical group CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 abstract 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical group [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 abstract 1
IPBVNPXQWQGGJP-UHFFFAOYSA-N acetic acid phenyl ester Natural products CC(=O)OC1=CC=CC=C1 IPBVNPXQWQGGJP-UHFFFAOYSA-N 0.000 abstract 1
229910052783 alkali metal Inorganic materials 0.000 abstract 1
229910001516 alkali metal iodide Inorganic materials 0.000 abstract 1
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
125000001246 bromo group Chemical group Br* 0.000 abstract 1
MCQSIFHQQMVWCK-UHFFFAOYSA-N bromo-(2-chlorophenyl)-iodomethanesulfonic acid Chemical group C1=CC=C(C(=C1)C(S(=O)(=O)O)(Br)I)Cl MCQSIFHQQMVWCK-UHFFFAOYSA-N 0.000 abstract 1
230000003197 catalytic effect Effects 0.000 abstract 1
125000001309 chloro group Chemical group Cl* 0.000 abstract 1
230000032050 esterification Effects 0.000 abstract 1
238000005886 esterification reaction Methods 0.000 abstract 1
125000005843 halogen group Chemical group 0.000 abstract 1
150000002431 hydrogen Chemical class 0.000 abstract 1
125000002346 iodo group Chemical group I* 0.000 abstract 1
238000004519 manufacturing process Methods 0.000 abstract 1
239000003960 organic solvent Substances 0.000 abstract 1
239000003444 phase transfer catalyst Substances 0.000 abstract 1
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 abstract 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
229940049953 phenylacetate Drugs 0.000 abstract 1
WLJVXDMOQOGPHL-UHFFFAOYSA-N phenylacetic acid Chemical class OC(=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-UHFFFAOYSA-N 0.000 abstract 1
229910052700 potassium Chemical group 0.000 abstract 1
239000011591 potassium Chemical group 0.000 abstract 1
229910052708 sodium Inorganic materials 0.000 abstract 1
239000011734 sodium Substances 0.000 abstract 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D505/00—Heterocyclic compounds containing 5-oxa-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. oxacephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D309/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
- C07D309/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D309/08—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D309/10—Oxygen atoms
- C07D309/12—Oxygen atoms only hydrogen atoms and one oxygen atom directly attached to ring carbon atoms, e.g. tetrahydropyranyl ethers

Landscapes

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

ES506788A 1980-11-03 1981-11-02 Un procedimiento para preparar un fenilacetato de bencilo. Expired ES8206431A1 (es)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US06/203,736 US4334079A (en)	1980-11-03	1980-11-03	Synthesis of substituted benzyl esters

Publications (2)

Publication Number	Publication Date
ES506788A0 true ES506788A0 (es)	1982-08-16
ES8206431A1 ES8206431A1 (es)	1982-08-16

Family

ID=22755118

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
ES506788A Expired ES8206431A1 (es)	1980-11-03	1981-11-02	Un procedimiento para preparar un fenilacetato de bencilo.

Country Status (9)

Country	Link
US (1)	US4334079A (es)
EP (1)	EP0051457B1 (es)
JP (1)	JPS57106643A (es)
AT (1)	ATE17113T1 (es)
DE (1)	DE3173330D1 (es)
DK (1)	DK482681A (es)
ES (1)	ES8206431A1 (es)
GB (1)	GB2086895B (es)
IE (1)	IE52059B1 (es)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3225290A1 (de) *	1982-07-07	1984-01-12	Merck Patent Gmbh	Ringverbindungen
JP2556026B2 (ja) *	1986-04-03	1996-11-20	日産化学工業株式会社	アルカリ廃水からの有用なカルボン酸の回収方法
US5084270A (en) *	1988-04-22	1992-01-28	Revlon, Inc.	Cosmetic compositions containing N-alkoxyalkylamides
FR2681595B1 (fr) *	1991-09-24	1994-09-02	Rhone Poulenc Chimie	Procede d'esterification de sels d'acides carboxyliques.
US9365486B2 (en) *	2014-07-01	2016-06-14	Muhammed Majeed	Synthesis of calebin-A and its biologically active analogs
KR102115644B1 (ko) *	2017-09-13	2020-05-27	주식회사 동도물산	7α-알콕시옥사세펨 중간체의 제조방법
CN112480147A (zh) *	2019-09-12	2021-03-12	杭州森泽医药科技有限公司	一种拉氧头孢中间体溶剂化物及其制备方法和表征
CN110885287B (zh) *	2019-12-04	2022-06-10	安徽圣诺贝化学科技有限公司	一种水杨酸钠合成水杨酸异辛酯的合成方法

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3035084A (en) *	1960-10-04	1962-05-15		Reaction rates of methallyl chloride with
US3651050A (en) *	1969-01-23	1972-03-21	Pfizer	Acylation of 6-aminopenicillanic acid and 7-aminocephalosporanic acid
GB1426557A (en) *	1972-10-05	1976-03-03	Beecham Group Ltd	Production of substituted monomalonate esters and their use in the production of alpha-carboxy penicillins and cephalosporins
DE2330838A1 (de) *	1973-06-16	1975-01-09	Thomae Gmbh Dr K	Neue carbonsaeureester von 3-(4biphenylyl)-1-butanolen und 3-(4-biphenylyl)2-buten-1-olen
JPS5228790B2 (es) *	1973-08-28	1977-07-28
GB1559799A (en) *	1975-11-12	1980-01-30	Shell Int Research	Process for preparing substituted benzylesters
DE2622456A1 (de) *	1976-05-20	1977-12-01	Bayer Ag	Verfahren zur herstellung von alpha-carboxybenzylpenicillin
DE2739854A1 (de) *	1977-09-03	1979-03-15	Bayer Ag	Fluorsubstituierte phenoxybenzyloxycarbonylderivate, verfahren zu ihrer herstellung und ihre verwendung als insektizide und akarizide

1980
- 1980-11-03 US US06/203,736 patent/US4334079A/en not_active Expired - Lifetime
1981
- 1981-10-29 EP EP81305140A patent/EP0051457B1/en not_active Expired
- 1981-10-29 GB GB8132619A patent/GB2086895B/en not_active Expired
- 1981-10-29 AT AT81305140T patent/ATE17113T1/de not_active IP Right Cessation
- 1981-10-29 DE DE8181305140T patent/DE3173330D1/de not_active Expired
- 1981-10-29 IE IE2539/81A patent/IE52059B1/en unknown
- 1981-11-02 JP JP56176303A patent/JPS57106643A/ja active Pending
- 1981-11-02 DK DK482681A patent/DK482681A/da not_active Application Discontinuation
- 1981-11-02 ES ES506788A patent/ES8206431A1/es not_active Expired

Also Published As

Publication number	Publication date
IE52059B1 (en)	1987-05-27
JPS57106643A (en)	1982-07-02
EP0051457A2 (en)	1982-05-12
ATE17113T1 (de)	1986-01-15
DK482681A (da)	1982-05-04
EP0051457A3 (en)	1982-09-15
ES8206431A1 (es)	1982-08-16
GB2086895A (en)	1982-05-19
EP0051457B1 (en)	1985-12-27
DE3173330D1 (en)	1986-02-06
GB2086895B (en)	1985-09-11
IE812539L (en)	1982-05-03
US4334079A (en)	1982-06-08

Publication	Publication Date	Title
KR890701519A (ko)	1989-12-20	하이드록시 방향족 화합물의 프로파르길 에테르를 제조하는 방법
ES506788A0 (es)	1982-08-16	Un procedimiento para preparar un fenilacetato de bencilo.
GB1481859A (en)	1977-08-03	Halogen-substituted benzimidazolone compounds and a process for their manufacture
BG35033A3 (en)	1984-01-16	Method for preparing o- metalyloxyphenol
KR920004397A (ko)	1992-03-27	1-옥사-3,8-디아자-4-옥소스피로[4,5]데칸 화합물의 제조방법.
US4577033A (en)	1986-03-18	Heterocyclic quaternary ammonium salts as phase transfer catalysts for aromatic ether imide preparation
GB1420185A (en)	1976-01-07	Nitrile-substituted o-ethyl-s-n-propyl-o-vinylthionothiol phosphoric acid esters a process for their preparation and their use as insecticides or acaraicides
ES8301195A1 (es)	1982-11-16	"un procedimiento para la preparacion de acido 2-(2,4-diclorofenoxi)fenilacetico".
FR2445314A1 (fr)	1980-07-25	Procede de preparation d'acide 2-(3-phenoxy-phenyl)-propionique
JPS5562053A (en)	1980-05-10	Production of aminophenol ether
JPS56118069A (en)	1981-09-16	8,9-dihydroxyphenanthridinium salt
GB1211275A (en)	1970-11-04	Process for the dehydrohalogenation of a beta-haloalkyl phosphonate
KR950017955A (ko)	1995-07-22	2, 4, 5-트리브로모피롤-3-카르보니트릴의 제조방법
JPS5668650A (en)	1981-06-09	Benzoic acid amide derivative
KR840003239A (ko)	1984-08-20	페녹시페녹시프로 피온산의 에스테르의 제조방법
ES8506606A1 (es)	1985-08-01	Procedimiento de preparacion de eteres oximas basicos y de sus sales de adicion acidas
JPS5659718A (en)	1981-05-23	Preparation of substituted phenoxycarboxylic acid derivative
JPS5626897A (en)	1981-03-16	Preparation of 4-nitro-substituted phenol o,o-dialkylthiophosphate
KR910003635B1 (ko)	1991-06-07	2-(2-나프틸옥시)프로피온아닐리드 유도체의 제조방법
JPS5545635A (en)	1980-03-31	Preparation of substituted diphenyl ether
JPS54112876A (en)	1979-09-04	Preparation of 1-substituted-1,4-dihydro-4-oxo-3-quinoline carboxylic acid derivatives
KR950702956A (ko)	1995-08-23	화학적 방법(chemical process)
JPS57212172A (en)	1982-12-27	Preparation of cyanuric halide derivative
UST102909I4 (en)	1983-04-05	Intermediates and process for insecticidal biphenylmethyl esters
KR930012676A (ko)	1993-07-21	할로말레인산 및 할로푸마르산 에스테르의 제조 방법