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Stannous Chloride → 2-Amino-5-(trifluoromethyl)phenol

HRID 323021
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HRID 323021 반응식
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([C:10]([F:13])([F:12])[F:11])=[CH:6][C:5]=1[OH:14])([O-])=O.Cl[Sn]Cl>CCO>[NH2:1][C:4]1[CH:9]=[CH:8][C:7]([C:10]([F:11])([F:12])[F:13])=[CH:6][C:5]=1[OH:14]
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참가 물질

4

반응물 2

HCID 24479Stannous ChlorideHCID 140916902-Nitro-5-(trifluoromethyl)phenol

생성물 1

HCID 155242772-Amino-5-(trifluoromethyl)phenol

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

2-Amino-5-trifluoromethylphenol was prepared by treating 2-nitro-5-trifluoromethylphenol (500 mg, 2.41 mmol) with a solution of SnCl2(3.5 g, mmol) in EtOH at 23° C. for 12 h. The mixture was concentrated to 50 mL and adjusted to pH 7 using saturated sodium bicarbonate. The reaction mixture was partitioned between H2O and EtOAc. The aqueous layer was separated and extracted with EtOAc. The combined organic extracts were dried over sodium sulfate, filtered and concentrated in vacuo. The resulting colorless oil (370 mg, 87%) was used without further purification. 1H NMR (CDCl3): 7.6 (s, 1H), 7.39 (d, 1H, J=8.5 Hz), 7.08 (d, 1H, J=8.5 Hz)

후처리

  1. concentrationThe mixture was concentrated to 50 mL
  2. customThe reaction mixture was partitioned between H2O and EtOAc
  3. customThe aqueous layer was separated
  4. extractionextracted with EtOAc
  5. dry with materialThe combined organic extracts were dried over sodium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo
  8. customThe resulting colorless oil (370 mg, 87%) was used without further purification

출처 및 근거

ORD 기록
ord-6f870a38b3e145f1b0789307f90892be
출처 데이터셋
uspto-grants-2001_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06211373B1

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