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(Diethylamino)sulfur trifluoride → 4-(4-Fluoropiperidin-1-yl)benzoic acid ethyl ester

HRID 1042388
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반응식

HRID 1042388 반응식
[CH2:1]([O:3][C:4](=[O:18])[C:5]1[CH:10]=[CH:9][C:8]([N:11]2[CH2:16][CH2:15][CH:14](O)[CH2:13][CH2:12]2)=[CH:7][CH:6]=1)[CH3:2].CCN(S(F)(F)[F:25])CC>ClCCl>[CH2:1]([O:3][C:4](=[O:18])[C:5]1[CH:10]=[CH:9][C:8]([N:11]2[CH2:16][CH2:15][CH:14]([F:25])[CH2:13][CH2:12]2)=[CH:7][CH:6]=1)[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 123472(Diethylamino)sulfur trifluorideHCID 12717445Ethyl 4-(4-hydroxypiperidin-1-yl)benzoate

생성물 1

HCID 686494674-(4-Fluoropiperidin-1-yl)benzoic acid ethyl ester수율 56%

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

To a solution of 4-(4-hydroxy-piperidin-1-yl)benzoic acid ethyl ester (1.25 g. 5 mmoles) in dry dichloromethane (30 ml) at room temperature under an inert atmosphere, it was slowly added DAST (0.97 g, 6 mmoles) in dichloromethane (5 ml). The reaction mixture was stirred at room temperature for 1 hour and then quenched with aqueous NaHCO3. The organic layer was washed with brine, dried and evaporated. The residue was purified by flash chromatography on silica gel using hexane/EtOAc (70/30) as eluent to give the title compound as a white solid (0.7 g, 56%).

후처리

  1. customat room temperature
  2. customquenched with aqueous NaHCO3
  3. washThe organic layer was washed with brine
  4. customdried
  5. customevaporated
  6. customThe residue was purified by flash chromatography on silica gel

출처 및 근거

ORD 기록
ord-b24f664b66c54749a85aebdf46621b1d
출처 데이터셋
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08557845B2

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