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4-[1-Cycloheptyl-methylidene]-2-(2,4,6-trimethyl-phenyl)-cyclopentane-1,3-dione → 4-Cycloheptylmethyl-2-(2,4,6-trimethyl-phenyl)-cyclopentane-1,3-dione

HRID 1631891
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HRID 1631891 반응식
[CH:1]1([CH:8]=[C:9]2[CH2:13][C:12](=[O:14])[CH:11]([C:15]3[C:20]([CH3:21])=[CH:19][C:18]([CH3:22])=[CH:17][C:16]=3[CH3:23])[C:10]2=[O:24])[CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1>CO.[Pd]>[CH:1]1([CH2:8][CH:9]2[CH2:13][C:12](=[O:14])[CH:11]([C:15]3[C:20]([CH3:21])=[CH:19][C:18]([CH3:22])=[CH:17][C:16]=3[CH3:23])[C:10]2=[O:24])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7]1
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참가 물질

4

반응물 1

HCID 668683574-[1-Cycloheptyl-methylidene]-2-(2,4,6-trimethyl-phenyl)-cyclopentane-1,3-dione

생성물 1

HCID 668847164-Cycloheptylmethyl-2-(2,4,6-trimethyl-phenyl)-cyclopentane-1,3-dione수율 74%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

To 5% w/w Pd/C (5 mg) was added a solution of 4-[1-Cycloheptyl-methylidene]-2-(2,4,6-trimethyl-phenyl)-cyclopentane-1,3-dione (39 mg, 0.12 mmol) in MeOH (10 ml). The reaction was stirred under an atmosphere of H2 (1.5 bar) for 2 hours, filtered through a pad of celite and washed through with MeOH (20 ml). The solvent was removed under reduced pressure to give the desired product as a colourless oil (29 mg) without need for further purification.

후처리

  1. filtrationfiltered through a pad of celite
  2. washwashed through with MeOH (20 ml)
  3. customThe solvent was removed under reduced pressure

출처 및 근거

ORD 기록
ord-8211cbb109b04d19a6860ff7e4f4f4a2
출처 데이터셋
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08791303B2

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