반응식
[CH:1](/[C:5]12[CH2:17][CH2:16][C:15](=[O:18])[C:14]([CH3:19])=[C:13]1[C:12]1[C:7](=[CH:8][C:9]([O:20]C)=[CH:10][CH:11]=1)[CH2:6]2)=[CH:2]\[CH2:3][CH3:4].Cl.N1C=CC=CC=1>>[CH:1](/[C:5]12[CH2:17][CH2:16][C:15](=[O:18])[C:14]([CH3:19])=[C:13]1[C:12]1[C:7](=[CH:8][C:9]([OH:20])=[CH:10][CH:11]=1)[CH2:6]2)=[CH:2]\[CH2:3][CH3:4]참가 물질
반응 조건
- 온도
- 190 °C
실험 절차
A mixture of 9a-[(1E)-1-butenyl]-7-methoxy-4-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-one (31.7 mg, 0.112 mmol) and pyridine hydrochloride (384 mg, 3.32 mmol) was placed under a nitrogen atmosphere and heated in an oil bath at 190° C. for 65 minutes. After cooling to room temperature, the reaction mixture was partitioned between water (4 ml) and EtOAc (10 mL). The organic phase was recovered, washed with brine (5 mL), dried over MgSO4, filtered, and evaporated under vacuum to an oil (30 mg). The crude product was purified by silica gel chromatography on a Biotage FLASH 12S column (1.2×7.5 cm), eluting with 3:1 hexanes-EtOAc. The product containing fractions were concentrated under vacuum and the residue lyophilized from benzene to provide 9a-[(1E)-1-butenyl]-7-hydroxy-4-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-one as a yellow, amorphous solid.
후처리
- temperatureAfter cooling to room temperature
- customthe reaction mixture was partitioned between water (4 ml) and EtOAc (10 mL)
- customThe organic phase was recovered
- washwashed with brine (5 mL)
- dry with materialdried over MgSO4
- filtrationfiltered
- customevaporated under vacuum to an oil (30 mg)
- customThe crude product was purified by silica gel chromatography on a Biotage FLASH 12S column (1.2×7.5 cm)
- washeluting with 3:1 hexanes-EtOAc
- additionThe product containing fractions
- concentrationwere concentrated under vacuum
출처 및 근거
- ORD 기록
- ord-d7b694b1a63448cfb05ba1ccd587d001
- 출처 데이터셋
- uspto-grants-2006_08
- 특허 번호
- US07087599B2
연결된 노트
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