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

HRID 436918
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HRID 436918 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]
참가 물질실험 절차후처리출처 및 근거반응 노트

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, b.p. 147°-150° C. (0.07 Torr).

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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, b.p. 147°-150° C. (0.07 Torr)

출처 및 근거

ORD 기록
ord-dcdbda06dbf04d1eabe3fab66d1d02ca
출처 데이터셋
uspto-grants-1977_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04028396

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