반응식
C([O:8][C:9]1[CH:10]=[CH:11][C:12]([C:16]2[CH2:25][CH2:24][C:19]3([O:23][CH2:22][CH2:21][O:20]3)[CH2:18][CH:17]=2)=[C:13]([OH:15])[CH:14]=1)C1C=CC=CC=1.O1CCCC1.C(O)C>ClCCl.[Pd]>[O:20]1[C:19]2([CH2:24][CH2:25][CH:16]([C:12]3[CH:11]=[CH:10][C:9]([OH:8])=[CH:14][C:13]=3[OH:15])[CH2:17][CH2:18]2)[O:23][CH2:22][CH2:21]1참가 물질
실험 절차
A round bottomed flask equipped with magnetic stirrer was charged with 5-(benzyloxy)-2-(1,4-dioxaspiro[4.5]dec-7-en-8-yl)phenol (14.5 g, 42.8 mmol) and tetrahydrofuran (50 ml). The stirred mixture was gently heated until a solution formed, after which the solution was allowed to cool to room temperature. Ethanol (100 ml) and palladium (4.54 g, 10% on activated carbon) were added sequentially. The reaction vessel was then evacuated, placed under a hydrogen atmosphere and stirred vigorously for 24 hr. The reaction mixture was filtered through a celite plug, washing with ethyl acetate. The filtrate was concentrated in vacuo to give an off white solid. The crude solid was slurried in dichloromethane (200 ml), then collected on a sinter, affording the title compound (10.2 g, 95%) as a white solid. m/z(ES+)251(M+H+).
후처리
- customA round bottomed flask equipped with magnetic stirrer
- temperatureThe stirred mixture was gently heated until a solution
- customformed
- customThe reaction vessel was then evacuated
- filtrationThe reaction mixture was filtered through a celite plug
- washwashing with ethyl acetate
- concentrationThe filtrate was concentrated in vacuo
- customto give an off white solid
- customcollected on a sinter
출처 및 근거
- ORD 기록
- ord-ee214bcd03d941fa890ad3d48d42534f
- 출처 데이터셋
- uspto-grants-2005_03
- 특허 번호
- US06861564B2
연결된 노트
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