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Methanol → (3R)-3-(4-Chlorophenyl)-3-cyclopropylpropanoic Acid

HRID 1835033
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HRID 1835033 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C@@H:8]([CH:12]2[CH2:14][CH2:13]2)[CH2:9][C:10]#N)=[CH:4][CH:3]=1.[OH-:15].[Na+].C[OH:18]>>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C@@H:8]([CH:12]2[CH2:14][CH2:13]2)[CH2:9][C:10]([OH:18])=[O:15])=[CH:4][CH:3]=1
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참가 물질

4

반응물 3

HCID 887MethanolHCID 14798Sodium HydroxideHCID 60104338(3R)-3-(4-chlorophenyl)-3-cyclopropylpropanenitrile

생성물 1

HCID 42073399(3R)-3-(4-Chlorophenyl)-3-cyclopropylpropanoic Acid수율 100%

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온도
0 °C

실험 절차

(3R)-3-(4-Chlorophenyl)-3-cyclopropylpropanenitrile (5.30 g, 25.8 mmol) is refluxed for 18 hours in a mixture of methanol (100 ml) and a 10% aqueous sodium hydroxide (100 ml). Methanol is removed in vacuo, the residual solution is cooled to 0° C. and acidified to pH 4 with concentrated hydrochloric acid. The aqueous layer is extracted with ethyl acetate (100 ml). The organic layer is dried over anhydrous sodium sulfate and concentrated in vacuo to afford the title compound as a colorless liquid (5.79 g, 100%) which is characterized by 1HNMR, IR and mass spectral analysis and used without further purification.

후처리

  1. customMethanol is removed in vacuo
  2. extractionThe aqueous layer is extracted with ethyl acetate (100 ml)
  3. dry with materialThe organic layer is dried over anhydrous sodium sulfate
  4. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-3c45b67a12414e509ee98ef033066cde
출처 데이터셋
uspto-grants-2004_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06770463B2

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