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p-Toluenesulfonic acid monohydrate → 2-(4-Carbethoxybutyl)cyclopentan-1-one

HRID 328821
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반응식

HRID 328821 반응식
[C:1]([CH2:4][CH2:5][CH2:6][CH2:7][CH:8]1[CH2:12][CH2:11][CH2:10][C:9]1=[O:13])([OH:3])=[O:2].O.[C:15]1(C)C=CC(S(O)(=O)=O)=C[CH:16]=1>C(O)C>[C:1]([CH2:4][CH2:5][CH2:6][CH2:7][CH:8]1[CH2:12][CH2:11][CH2:10][C:9]1=[O:13])([O:3][CH2:15][CH3:16])=[O:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 521998p-Toluenesulfonic acid monohydrateHCID 135134014-Carboxybutylcyclopentan-1-one

생성물 1

HCID 130462922-(4-Carbethoxybutyl)cyclopentan-1-one

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A stirred solution of 124 g. (0.673 mole) of 2-(4-carboxybutyl)cyclopentan-1-one (Example 2), 800 ml. of ethanol and 1 g. of p-toluenesulfonic acid monohydrate is heated at reflux for 18 hours. The solvent is evaporated and the residue is dissolved in ether. The ether solution is washed with saline, dilute sodium bicarbonate solution and again with saline, dried over magnesium sulfate and evaporated. The oil is distilled under reduced pressure to give 149 g. of a colorless oil, b.p. 106°-109° C. (0.23 mm).

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후처리

  1. temperatureat reflux for 18 hours
  2. customThe solvent is evaporated
  3. dissolutionthe residue is dissolved in ether
  4. washThe ether solution is washed with saline, dilute sodium bicarbonate solution and again with saline
  5. dry with materialdried over magnesium sulfate
  6. customevaporated
  7. distillationThe oil is distilled under reduced pressure
  8. customto give 149 g

출처 및 근거

ORD 기록
ord-38b72d3f102241d79f73215e597750d9
출처 데이터셋
uspto-grants-1977_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04018811

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