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Hydrochloric Acid → Methyl(3R)-3-(4-chlorophenyl)-3-cyclopropylpropanoate

HRID 1835034
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HRID 1835034 반응식
Cl.[Cl:2][C:3]1[CH:8]=[CH:7][C:6]([C@@H:9]([CH:14]2[CH2:16][CH2:15]2)[CH2:10][C:11]([OH:13])=[O:12])=[CH:5][CH:4]=1.[CH3:17]O>>[Cl:2][C:3]1[CH:4]=[CH:5][C:6]([C@@H:9]([CH:14]2[CH2:15][CH2:16]2)[CH2:10][C:11]([O:13][CH3:17])=[O:12])=[CH:7][CH:8]=1
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참가 물질

4

반응물 3

HCID 313Hydrochloric AcidHCID 887MethanolHCID 42073399(3R)-3-(4-Chlorophenyl)-3-cyclopropylpropanoic Acid

생성물 1

HCID 70125923Methyl(3R)-3-(4-chlorophenyl)-3-cyclopropylpropanoate수율 84%

실험 절차

Hydrogen chloride gas is bubbled into a solution of (3R)-3-(4-chlorophenyl)-3-cyclopropylpropanoic acid (5.79 g, 25.85 mmol) in methanol (100 ml) at 0° C. for 30 seconds. The solution is allowed to warm to room temperature and stirred for 18 hours. The solution is concentrated in vacuo, diluted with chloroform (100 ml) and washed with 5% aqueous sodium bicarbonate (100 ml). The organic layer is dried over anhydrous sodium sulfate and concentrated in vacuo. The residue is chromatographed on silica gel eluting with ether:hexane (10:90) to yield the title compound as a colorless liquid (5.15 g, 84% from (3R)-3-(4-chlorophenyl)-3-cyclopropylpropanenitrile) which is characterized by 1HNMR, IR and mass spectral analyses.

후처리

  1. concentrationThe solution is concentrated in vacuo
  2. additiondiluted with chloroform (100 ml)
  3. washwashed with 5% aqueous sodium bicarbonate (100 ml)
  4. dry with materialThe organic layer is dried over anhydrous sodium sulfate
  5. concentrationconcentrated in vacuo
  6. customThe residue is chromatographed on silica gel eluting with ether:hexane (10:90)

출처 및 근거

ORD 기록
ord-686ab34f513c4e20ab389f09acaceed3
출처 데이터셋
uspto-grants-2004_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06770463B2

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