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4H-pyran-4-one → N-[3-(Trifluoromethoxy)benzyl]tetrahydro-2H-pyran-4-amine

HRID 467952
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인쇄 미리보기

반응식

HRID 467952 반응식
O=[C:2]1[CH:7]=[CH:6][O:5][CH:4]=[CH:3]1.[F:8][C:9]([F:20])([F:19])[O:10][C:11]1[CH:12]=[C:13]([CH:16]=[CH:17][CH:18]=1)[CH2:14][NH2:15].C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+].[OH-].[Na+]>C(Cl)(Cl)Cl>[F:8][C:9]([F:19])([F:20])[O:10][C:11]1[CH:12]=[C:13]([CH:16]=[CH:17][CH:18]=1)[CH2:14][NH:15][CH:2]1[CH2:7][CH2:6][O:5][CH2:4][CH2:3]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 79684H-pyran-4-oneHCID 14798Sodium HydroxideHCID 1452643-(Trifluoromethoxy)benzylamineHCID 5049666Sodium triacetoxyborohydride

생성물 1

HCID 58049381N-[3-(Trifluoromethoxy)benzyl]tetrahydro-2H-pyran-4-amine수율 82.2%

시약·촉매·용매 1

HCID 6212
Chloroform
용매

실험 절차

To a solution of 4-oxo-1H-pyran (200 mg) in chloroform (2 mL), 3-trifluoromethoxybenzylamine (380 mg) was added and the resulting mixture was stirred at room temperature for 30 minutes. Sodium (triacetoxy)borohydride (850 mg) was added and the resulting mixture was stirred for an hour. To the reaction mixture, an aqueous solution of 6 M sodium hydroxide was added and extraction was conducted with ethyl acetate. The solvents were distilled off under reduced pressure and the resulting residue was purified by column chromatography (NH silica gel cartridge; hexane/ethyl acetate=9:1 to 1:9) to give the titled compound (450 mg).

후처리

  1. stirringthe resulting mixture was stirred for an hour
  2. extractionextraction
  3. distillationThe solvents were distilled off under reduced pressure
  4. customthe resulting residue was purified by column chromatography (NH silica gel cartridge; hexane/ethyl acetate=9:1 to 1:9)

출처 및 근거

ORD 기록
ord-8db1cfc7e3bc43d68e79f29d8b8cd4c2
출처 데이터셋
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08623898B2

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