1,4-Cyclohexanedione → 4-Benzylcyclohexanone

HRID 67686노트

반응식

HRID 67686 반응식
[C:1]1(=O)[CH2:6][CH2:5][C:4](=[O:7])[CH2:3][CH2:2]1.[CH:9](=P(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1>>[CH2:9]([CH:1]1[CH2:2][CH2:3][C:4](=[O:7])[CH2:5][CH2:6]1)[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1.[CH:9](=[C:1]1[CH2:2][CH2:3][C:4](=[O:7])[CH2:5][CH2:6]1)[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1

참가 물질

4

실험 절차

4-Benzylcyclohexanone is prepared as follows. Cyclohexane-1,4-dione, ethylene monoketal is reacted with benzylidenetriphenylphosphorane to afford 4-benzylidenecyclohexanone, ethylene ketal, which is catalytically hydrogenated, e.g., using palladium on carbon, to give 4-benzylcyclohexanone, ethylene ketal. Deketalization with mineral acid, e.g., hydrochloric acid in acetone solution, provides 4-benzylcyclohexanone.

출처 및 근거

ORD 기록
ord-26c845544319411aa46c1de7ef28329b
출처 데이터셋
uspto-grants-1982_08
특허 번호
US04346101

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