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p-Toluenesulfonic acid → Ethyl {[5-(5-oxocyclopent-1-en-1-yl)pentyl]sulfanyl}acetate

HRID 1447944
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HRID 1447944 반응식
[C:1]([CH2:4][S:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][C:11]1[C:12](=[O:16])[CH2:13][CH2:14][CH:15]=1)([OH:3])=[O:2].[C:17]1(C)C=CC(S(O)(=O)=O)=C[CH:18]=1>C(O)C>[C:1]([CH2:4][S:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][C:11]1[C:12](=[O:16])[CH2:13][CH2:14][CH:15]=1)([O:3][CH2:17][CH3:18])=[O:2]
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참가 물질

4

반응물 2

HCID 6101p-Toluenesulfonic acidHCID 20347252{[5-(5-Oxocyclopent-1-en-1-yl)pentyl]sulfanyl}acetic acid

생성물 1

HCID 20347243Ethyl {[5-(5-oxocyclopent-1-en-1-yl)pentyl]sulfanyl}acetate

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A mixture of 74 g. (0.306 mols) of 2-(7-carboxy-6-thiaheptyl)-2-cyclopentenone, 1200 ml. of ethanol and 1 g. p-toluenesulfonic acid is stirred and refluxed for 18 hours. The resulting solution is concentrated and the residue is dissolved in ether. The organic phase is washed with water, sodium bicarbonate solution and saline, dried (MgSO4) and evaporated. The residue is distilled to give a light yellow oil, o.p. 147°-150° C. (0.07 Torr).

후처리

  1. additionA mixture of 74 g
  2. temperaturerefluxed for 18 hours
  3. concentrationThe resulting solution is concentrated
  4. dissolutionthe residue is dissolved in ether
  5. washThe organic phase is washed with water, sodium bicarbonate solution and saline
  6. dry with materialdried (MgSO4)
  7. customevaporated
  8. distillationThe residue is distilled
  9. customto give a light yellow oil, o.p
  10. custom147°-150° C. (0.07 Torr)

출처 및 근거

ORD 기록
ord-844498fe1b6e403285e0153c0ecfeeab
출처 데이터셋
uspto-grants-1979_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04178461

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