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Sodium Dithionite → 2-Amino-6-chloro-4-(trifluoromethyl)phenol

HRID 649098
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HRID 649098 반응식
S(S([O-])=O)([O-])=O.[Na+].[Na+].[Cl:9][C:10]1[CH:15]=[C:14]([C:16]([F:19])([F:18])[F:17])[CH:13]=[C:12]([N+:20]([O-])=O)[C:11]=1[OH:23]>C(O)C.O>[NH2:20][C:12]1[CH:13]=[C:14]([C:16]([F:17])([F:18])[F:19])[CH:15]=[C:10]([Cl:9])[C:11]=1[OH:23]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 24489Sodium DithioniteHCID 538287782-Chloro-6-nitro-4-(trifluoromethyl)phenol

생성물 1

HCID 212870732-Amino-6-chloro-4-(trifluoromethyl)phenol

시약·촉매·용매 2

HCID 702Ethanol용매HCID 962Water용매

실험 절차

Solid sodium dithionite (10 g) was added in portions to a stirred solution of 2-chloro-6-nitro-4-trifluoromethylphenol (4.5 g) in a mixture of ethanol (20 ml) and water (30 ml). The solution was stirred for 2 hours, left overnight, filtered, and evaporated. The residue was mixed with toluene and the toluene removed under reduced pressure. The residue was extracted with boiling chloroform (3×100 ml) and the chloroform extracts evaporated to give a yellow oil identified as the required substituted phenol.

후처리

  1. waitleft overnight
  2. filtrationfiltered
  3. customevaporated
  4. additionThe residue was mixed with toluene
  5. customthe toluene removed under reduced pressure
  6. extractionThe residue was extracted with boiling chloroform (3×100 ml)
  7. customthe chloroform extracts evaporated
  8. customto give a yellow oil

출처 및 근거

ORD 기록
ord-860de3247fae46ec987f818a8ff9fc4d
출처 데이터셋
uspto-grants-1988_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04738711

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