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Thionyl Chloride → 3-Nitro-5-(trifluoromethyl)benzoyl chloride

HRID 1042655
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반응식

HRID 1042655 반응식
[N+:1]([C:4]1[CH:5]=[C:6]([CH:10]=[C:11]([C:13]([F:16])([F:15])[F:14])[CH:12]=1)[C:7](O)=[O:8])([O-:3])=[O:2].S(Cl)([Cl:19])=O>>[N+:1]([C:4]1[CH:5]=[C:6]([CH:10]=[C:11]([C:13]([F:16])([F:15])[F:14])[CH:12]=1)[C:7]([Cl:19])=[O:8])([O-:3])=[O:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 24386Thionyl ChlorideHCID 6166023-Nitro-5-(trifluoromethyl)benzoic acid

생성물 1

HCID 226083993-Nitro-5-(trifluoromethyl)benzoyl chloride

실험 절차

A solution of thionyl chloride (30 ml) and 3-nitro-5-(trifluoromethyl)benzoic acid (10 g) was heated to reflux for 2 h. The reaction mixture was concentrated under reduced pressure and azeotroped with toluene (10 ml—removed under reduced pressure) to afford 3-nitro-5-(trifluoromethyl)benzoyl chloride.

후처리

  1. temperatureto reflux for 2 h
  2. concentrationThe reaction mixture was concentrated under reduced pressure
  3. customazeotroped with toluene (10 ml—removed under reduced pressure)

출처 및 근거

ORD 기록
ord-8c96f968b55f49029bd9be4cd9d70eef
출처 데이터셋
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08557996B2

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