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Triphenylphosphine → [4-(4-Fluorophenoxy]butyl]triphenylphosphonium bromide

HRID 384443
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HRID 384443 반응식
[Br:1][CH2:2][CH2:3][CH2:4][CH2:5][O:6][C:7]1[CH:12]=[CH:11][C:10]([F:13])=[CH:9][CH:8]=1.[C:14]1([P:20]([C:27]2[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=2)[C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1>C1(C)C=CC=CC=1>[Br-:1].[F:13][C:10]1[CH:11]=[CH:12][C:7]([O:6][CH2:5][CH2:4][CH2:3][CH2:2][P+:20]([C:21]2[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=2)([C:27]2[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=2)[C:14]2[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=2)=[CH:8][CH:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 11776TriphenylphosphineHCID 71722951-(4-Bromobutoxy)-4-fluorobenzene

생성물 1

HCID 86646233[4-(4-Fluorophenoxy]butyl]triphenylphosphonium bromide수율 39%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

A solution of 1-(4-bromobutoxy)-4-fluorobenzene (2.56 g) and triphenylphosphine (2.72 g) in toluene (10 mL) was heated under reflux for 24 hours. The reaction mixture was allowed to cool to room temperature, and the precipitated solid was collected by filtration and dried to obtain [4-(4-fluorophenoxy]butyl]triphenylphosphonium bromide (2.06 g).

후처리

  1. temperatureunder reflux for 24 hours
  2. filtrationthe precipitated solid was collected by filtration
  3. customdried

출처 및 근거

ORD 기록
ord-59efe31c65a04734b362801348bba2d4
출처 데이터셋
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08367702B2

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