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Water → 3-Cyclopentyloxy-4-(methylthio)benzoic acid

HRID 356949
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HRID 356949 반응식
[CH:1]1([O:6][C:7]2[CH:8]=[C:9]([CH:14]=[CH:15][C:16]=2[S:17][CH3:18])[C:10]([O:12]C)=[O:11])[CH2:5][CH2:4][CH2:3][CH2:2]1.O.C(=O)([O-])[O-].[K+].[K+]>CO>[CH:1]1([O:6][C:7]2[CH:8]=[C:9]([CH:14]=[CH:15][C:16]=2[S:17][CH3:18])[C:10]([OH:12])=[O:11])[CH2:2][CH2:3][CH2:4][CH2:5]1
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참가 물질

5

반응물 3

HCID 962WaterHCID 11430Potassium CarbonateHCID 21187944Methyl 3-cyclopentyloxy-4-(methylthio)benzoate

생성물 1

HCID 211878293-Cyclopentyloxy-4-(methylthio)benzoic acid

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A suspension of methyl 3-cyclopentyloxy-4-(methylthio)benzoate (0.8 g; that is prepared as described in Reference Example 54) in methanol (10 mL) and water (5 mL) is treated with potassium carbonate (0.48 g) and the mixture is heated at reflux for 7 hours. The mixture is concentrated, and the resulting residue is partitioned between diethyl ether (20 mL) and water (20 mL). The aqueous layer is separated, acidified to pH 1 by treatment with dilute hydrochloric acid (2 N), and extracted with dichloromethane (2×25 mL). The combined organic extracts are dried and concentrated, to give 3-cyclopentyloxy-4-(methylthio)benzoic acid (0.7 g) in the form of a white solid m.p. 150°-152° C.

후처리

  1. customthat is prepared
  2. temperaturethe mixture is heated
  3. temperatureat reflux for 7 hours
  4. concentrationThe mixture is concentrated
  5. customthe resulting residue is partitioned between diethyl ether (20 mL) and water (20 mL)
  6. customThe aqueous layer is separated
  7. extractionextracted with dichloromethane (2×25 mL)
  8. customThe combined organic extracts are dried
  9. concentrationconcentrated

출처 및 근거

ORD 기록
ord-3d6cf4c6bd4247f2b9abc62a9e7f655e
출처 데이터셋
uspto-grants-1998_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05840724

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