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Thionyl Chloride → 1-[(4-Bromophenyl)chloromethyl]-3-methoxybenzene

HRID 893289
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인쇄 미리보기

반응식

HRID 893289 반응식
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([C:10]2[CH:15]=[CH:14][CH:13]=[C:12]([O:16][CH3:17])[CH:11]=2)O)=[CH:4][CH:3]=1.S(Cl)([Cl:20])=O>ClCCl>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([Cl:20])[C:10]2[CH:15]=[CH:14][CH:13]=[C:12]([O:16][CH3:17])[CH:11]=2)=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24386Thionyl ChlorideHCID 18507125HCID 18507125, 화합물

생성물 1

HCID 189559361-[(4-Bromophenyl)chloromethyl]-3-methoxybenzene

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

The crude alcohol from above (6.5 g, 22 mmole) was dissolved in 50 ml of dichloromethane, and 2.4 ml (33 mmole) of thionyl chloride was added dropwise at room temperature. The reaction was allowed to stir overnight and the solvent was removed under vacuum. The crude product was redissolved in 50 ml of toluene and the solvent was again removed under vacuum in order to eliminate excess thionyl chloride, providing 6.85 g of crude 4-bromo-3'-methoxybenzhydryl chloride as a dark oil.

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  1. customthe solvent was removed under vacuum
  2. dissolutionThe crude product was redissolved in 50 ml of toluene
  3. customthe solvent was again removed under vacuum in order

출처 및 근거

ORD 기록
ord-c3688242e5cb4b27a3ab26a15a04bae7
출처 데이터셋
uspto-grants-1992_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05124330

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