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Potassium Carbonate → 3-Cyclopentyloxy-4-(methylthio)benzoic acid

HRID 356921
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HRID 356921 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.C(=O)([O-])[O-].[K+].[K+]>CO.O>[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 2

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

생성물 1

HCID 211878293-Cyclopentyloxy-4-(methylthio)benzoic acid수율 92.4%

시약·촉매·용매 2

HCID 887Methanol용매HCID 962Water용매

실험 절차

A suspension of methyl 3-cyclopentyloxy-4-(methylthio)benzoate (0.8 g) 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. temperaturethe mixture is heated
  2. temperatureat reflux for 7 hours
  3. concentrationThe mixture is concentrated
  4. customthe resulting residue is partitioned between diethyl ether (20 mL) and water (20 mL)
  5. customThe aqueous layer is separated
  6. extractionextracted with dichloromethane (2×25 mL)
  7. customThe combined organic extracts are dried
  8. concentrationconcentrated

출처 및 근거

ORD 기록
ord-95353bba5c8147ad9e9bc6d68f2ba522
출처 데이터셋
uspto-grants-1998_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05840724

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