Triphenylphosphine → (3-Methylbut-2-enyl)triphenylphosphonium bromide

HRID 1073689

반응식

HRID 1073689 반응식
[CH3:1][C:2]([CH3:6])=[CH:3][CH2:4][Br:5].[C:7]1([P:13]([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1>C1(C)C=CC=CC=1>[Br-:5].[CH3:1][C:2]([CH3:6])=[CH:3][CH2:4][P+:13]([C:14]1[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=1)([C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)[C:7]1[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=1

참가 물질

4

실험 절차

A mixture of 3,3-dimethylallyl bromide (50.0 g), triphenylphosphine (88.0 g) and dry toluene (500 ml) was stirred and heated at the reflux temperature for one hour, and then kept at the ambient temperature for 18 hours. The white precipitate of 3,3-dimethylall-yl triphenylphosphonium bromide (m.p. 242° C.) was collected by filtration, washed with diethyl ether and dried.

후처리

  1. temperatureheated at the reflux temperature for one hour
  2. filtrationThe white precipitate of 3,3-dimethylall-yl triphenylphosphonium bromide (m.p. 242° C.) was collected by filtration
  3. washwashed with diethyl ether
  4. customdried

출처 및 근거

ORD 기록
ord-3f4384b5fe984591a934eb49c1c3c893
출처 데이터셋
uspto-grants-1990_11
특허 번호
US04970330

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