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Trimethyl phosphite → 1-(Benzothiazol-2-yl)-4-dimethoxyphosphinylmethylbenzene

HRID 224316
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인쇄 미리보기

반응식

HRID 224316 반응식
[S:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[C:10]1[CH:15]=[CH:14][C:13]([CH2:16]Br)=[CH:12][CH:11]=1.[P:18]([O:23]C)([O:21][CH3:22])[O:19][CH3:20]>>[S:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[C:10]1[CH:15]=[CH:14][C:13]([CH2:16][P:18]([O:21][CH3:22])([O:19][CH3:20])=[O:23])=[CH:12][CH:11]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 8472Trimethyl phosphiteHCID 132767292-(4-(Bromomethyl)phenyl)benzo[d]thiazole

생성물 1

HCID 135992101-(Benzothiazol-2-yl)-4-dimethoxyphosphinylmethylbenzene

실험 절차

6.08 g (0.2 mol) of 4-(benzothiazol-2-yl) bromomethylbenzene was reacted with 10 ml of trimethyl phosphite in nitrogen gas at 130°-160° C. for 15 minutes. The reaction mixture was allowed to cool down to room temperature and the resulting crystals were crystallized from n-hexane to give 3.9 g (83%) of colorless flakes of 1-(benzothiazol-2-yl)-4-dimethoxyphosphinylmethylbenzene melting at 129.5°-130.5° C.

후처리

  1. customthe resulting crystals were crystallized from n-hexane

출처 및 근거

ORD 기록
ord-af63bdd480874f3b9724ea1a733a4288
출처 데이터셋
uspto-grants-1980_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04232010

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