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m-Chloroperbenzoic acid → HCID 53880775, 화합물

HRID 258883
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반응식

HRID 258883 반응식
[CH3:1][N:2]([CH2:4][C:5]#[C:6][C:7]1[C:13]2[CH:14]=[C:15]([Cl:18])[CH:16]=[CH:17][C:12]=2[S:11][C:10]2[CH:19]=[CH:20][CH:21]=[CH:22][C:9]=2[CH:8]=1)[CH3:3].ClC1C=CC=C(C(OO)=[O:31])C=1>C(Cl)(Cl)Cl>[CH3:1][N+:2]([O-:31])([CH2:4][C:5]#[C:6][C:7]1[C:13]2[CH:14]=[C:15]([Cl:18])[CH:16]=[CH:17][C:12]=2[S:11][C:10]2[CH:19]=[CH:20][CH:21]=[CH:22][C:9]=2[CH:8]=1)[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 70297m-Chloroperbenzoic acidHCID 21424941HCID 21424941, 화합물

생성물 1

HCID 53880775HCID 53880775, 화합물

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

A solution of 2 g. of N,N-dimethyl-3-(8-chloro-dibenzo [b,f]thiepin-10-yl)-2-propynylamine in 100 ml. chloroform is treated at -50° C. with 1.2 g. of m-chloroperbenzoic acid. The solution is stirred for 15 minutes at this temperature, warmed to room temperature and chromatographed on basic aluminum oxide using chloroform/methanol (9:1) as the eluant, whereby there is obtained N,N-dimethyl-3-(8-chloro-dibenzo [b,f]thiepin-10-yl)-2-propynylamine N-oxide, which melts at 68°-69° C. after recrystallization from ethyl acetate/petroleum ether.

후처리

  1. customchromatographed on basic aluminum oxide

출처 및 근거

ORD 기록
ord-521690fd26544084906578e1ef9aeedd
출처 데이터셋
uspto-grants-1977_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04035386

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