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Water → (2-Chloro-3-trifluoromethyl-benzyl)-(2-thiophen-2-yl-propyl)-amine

HRID 902682
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HRID 902682 반응식
[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[CH:6]([CH3:9])[CH:7]=O.[Cl:10][C:11]1[C:18]([C:19]([F:22])([F:21])[F:20])=[CH:17][CH:16]=[CH:15][C:12]=1[CH2:13][NH2:14].C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+].O>ClCCl.CCCCCC>[Cl:10][C:11]1[C:18]([C:19]([F:20])([F:21])[F:22])=[CH:17][CH:16]=[CH:15][C:12]=1[CH2:13][NH:14][CH2:7][CH:6]([C:2]1[S:1][CH:5]=[CH:4][CH:3]=1)[CH3:9]
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참가 물질

7

반응물 4

HCID 962WaterHCID 5049666Sodium triacetoxyborohydrideHCID 52242072-Chloro-3-(trifluoromethyl)benzylamineHCID 110517432-(Thiophen-2-yl)propanal

생성물 1

HCID 69253724(2-Chloro-3-trifluoromethyl-benzyl)-(2-thiophen-2-yl-propyl)-amine수율 107%

시약·촉매·용매 2

HCID 6344
Dichloromethane
용매
HCID 8058Hexane용매

실험 절차

To a solution of 2-thiophen-2-yl-propionaldehyde (100 mg, 0.7 mmol) in dry dichloromethane (20 ml) was added 2-chloro-3-trifluoromethyl-benzylamine (30 mg, 0.14 mmol) followed by the addition of sodium triacetoxyborohydride (60.5 mg, 0.28 mmol). After the resulting mixture was stirred at room temperature overnight water was added to quench the reaction. The aqueous layer was extracted with ethyl acetate. The combined organic layers was washed with brine, dried over sodium sulfate and concentrated in vacco. The crude mixture was purified by silica gel column chromatograph using EtOAc:Hexane/25:75 as the eluent to give 50 mg (40% yield) of the title compound as an oil. MS m/e 334.4 (M+H)+.

후처리

  1. additionwas added
  2. customto quench
  3. customthe reaction
  4. extractionThe aqueous layer was extracted with ethyl acetate
  5. washThe combined organic layers was washed with brine
  6. dry with materialdried over sodium sulfate
  7. concentrationconcentrated in vacco
  8. customThe crude mixture was purified by silica gel column chromatograph

출처 및 근거

ORD 기록
ord-8ee8eb59e042489ea95fc8c016eb9639
출처 데이터셋
uspto-grants-2008_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07365085B2

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