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Triethyl phosphite → 5-(2-Chloro-4-trifluoromethylphenoxy)benzo-2,1,3-oxadiazole

HRID 463599
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HRID 463599 반응식
[Cl:1][C:2]1[CH:18]=[C:17]([C:19]([F:22])([F:21])[F:20])[CH:16]=[CH:15][C:3]=1[O:4][C:5]1[CH:14]=[CH:13][C:8]2=[N+:9]([O-])[O:10][N:11]=[C:7]2[CH:6]=1.P(OCC)(OCC)OCC>C(O)C>[Cl:1][C:2]1[CH:18]=[C:17]([C:19]([F:22])([F:20])[F:21])[CH:16]=[CH:15][C:3]=1[O:4][C:5]1[CH:14]=[CH:13][C:8]2=[N:9][O:10][N:11]=[C:7]2[CH:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 31215Triethyl phosphiteHCID 135343365-(2-chloro-4-trifluoromethylphenoxy)benzo-2,1,3-oxadiazole N-oxide

생성물 1

HCID 135343375-(2-Chloro-4-trifluoromethylphenoxy)benzo-2,1,3-oxadiazole

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A mixture of 5-(2-chloro-4-trifluoromethylphenoxy)benzo-2,1,3-oxadiazole N-oxide (2.0 g) and triethyl phosphite (10 ml) is heated under reflux in ~150 ml of ethanol for 4 hours. The reaction is cooled and stripped, and the crude product is purified by prep. TLC (15% ethyl acetate/hexane) to give 5-(2-chloro-4-trifluoromethylphenoxy)benzo-2,1,3-oxadiazole, m.p. 65°-66°.

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후처리

  1. temperatureis heated
  2. temperatureThe reaction is cooled
  3. customthe crude product is purified by prep

출처 및 근거

ORD 기록
ord-cf310e67826c4446abb932517a161b5c
출처 데이터셋
uspto-grants-1985_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04544400

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