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Triethylamine → 2-(4-Fluoro-3-methyl-phenylsulfanyl)-hexanoic acid methyl ester

HRID 1361050
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HRID 1361050 반응식
[CH3:1][O:2][C:3](=[O:10])[CH:4](Br)[CH2:5][CH2:6][CH2:7][CH3:8].[F:11][C:12]1[CH:17]=[CH:16][C:15]([SH:18])=[CH:14][C:13]=1[CH3:19].C(N(CC)CC)C>ClCCl>[CH3:1][O:2][C:3](=[O:10])[CH:4]([S:18][C:15]1[CH:16]=[CH:17][C:12]([F:11])=[C:13]([CH3:19])[CH:14]=1)[CH2:5][CH2:6][CH2:7][CH3:8]
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참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 95578Hexanoic acid, 2-bromo-, methyl esterHCID 27590424-Fluoro-3-methylbenzene-1-thiol

생성물 1

HCID 597751732-(4-Fluoro-3-methyl-phenylsulfanyl)-hexanoic acid methyl ester수율 92%

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

To a solution of 2-bromo-hexanoic acid methyl ester (0.500 g, 2.404 mmol) and 4-fluoro-3-methyl-benzenethiol (0.340 g, 2.404 mmol) in 20 mL of dichloromethane, was added triethylamine (3.3 mL, 12.020 mmol). After stirring at room temperature under N2 for 46 h, the reaction mixture was diluted with dichloromethane and washed with 1N HCl and brine. The organic layer dried over anhydrous Na2SO4. After removing the solvent under reduced pressure, the product was isolated by Flash chromatography (silica gel) eluting with 0-20% ethyl acetate/hexanes to give the title compound as colorless oil (0.596 g, 92% yield). LC-MS: tR=11.2 min; m/z 271 (M+H)+.

후처리

  1. washwashed with 1N HCl and brine
  2. dry with materialThe organic layer dried over anhydrous Na2SO4
  3. customAfter removing the solvent under reduced pressure
  4. customthe product was isolated by Flash chromatography (silica gel)
  5. washeluting with 0-20% ethyl acetate/hexanes

출처 및 근거

ORD 기록
ord-370248bfd41946c3800a5f138ec30ae8
출처 데이터셋
uspto-grants-2011_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07879911B2

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