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2-Cyclopenten-1-one → 5,6-Diphenyl-2,3,3a,4,7,7a-hexahydro-1H-inden-1-one

HRID 351448
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인쇄 미리보기

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HRID 351448 반응식
[C:1]1([C:7]([C:9]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)=[CH2:10])=[CH2:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[C:17]1(=[O:22])[CH2:21][CH2:20][CH:19]=[CH:18]1>C1(C)C=CC=CC=1>[C:1]1([C:7]2[CH2:8][CH:20]3[CH:21]([CH2:10][C:9]=2[C:11]2[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=2)[C:17](=[O:22])[CH2:18][CH2:19]3)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 135882-Cyclopenten-1-oneHCID 41291332,3-Diphenylbuta-1,3-diene

생성물 1

HCID 184363635,6-Diphenyl-2,3,3a,4,7,7a-hexahydro-1H-inden-1-one

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

A mixture of 2,3-diphenyl-1,3-butadiene (2.772 g, 13.44 mmol) and cyclopent-2-enone (1 eq.) was refluxed in toluene (26 mL) for 48 h. The reaction mixture was then concentrated and purified on SiO2 (20% ethyl acetate/hexane) to yield 5,6-diphenyl-2,3,3a,4,7,7a-hexahydro-inden-1-one.

후처리

  1. concentrationThe reaction mixture was then concentrated
  2. custompurified on SiO2 (20% ethyl acetate/hexane)

출처 및 근거

ORD 기록
ord-7c19c55ba5554137b65b9aace25a9630
출처 데이터셋
uspto-grants-2007_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07183445B2

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