Hydrogen Bromide → (+)-5,6-Dimethoxy-2-[2,2,4,6,7-pentamethyl-3-(4-methylphenyl)-2,3-dihydro-1-benzofuran-5-yl]isoindoline hydrobromide
반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][C:11]=1[O:12][CH3:13])[CH2:8][N:7]([C:14]1[C:15]([CH3:34])=[C:16]([CH3:33])[C:17]3[O:21][C:20]([CH3:23])([CH3:22])[CH:19]([C:24]4[CH:29]=[CH:28][C:27]([CH3:30])=[CH:26][CH:25]=4)[C:18]=3[C:31]=1[CH3:32])[CH2:6]2.[BrH:35]>C(O)(=O)C>[BrH:35].[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][C:11]=1[O:12][CH3:13])[CH2:8][N:7]([C:14]1[C:15]([CH3:34])=[C:16]([CH3:33])[C:17]3[O:21][C:20]([CH3:23])([CH3:22])[CH:19]([C:24]4[CH:25]=[CH:26][C:27]([CH3:30])=[CH:28][CH:29]=4)[C:18]=3[C:31]=1[CH3:32])[CH2:6]2참가 물질
4
반응물 2
생성물 1
시약·촉매·용매 1
실험 절차
(+)-5,6-Dimethoxy-2-[2,2,4,6,7-pentamethyl-3-(4-methylphenyl)-2,3-dihydro-1-benzofuran-5-yl]isoindoline (150 mg, 0.327 mmol) was dissolved into a 25% solution of hydrogen bromide in acetic acid and the mixture was concentrated under reduced pressure. The residue was crystallized from methanol to obtain 92 mg (52% yield) of the title compound. Melting point: 174-177° C. [α]D=+40.2° (c=0.495, methanol)
후처리
- concentrationthe mixture was concentrated under reduced pressure
- customThe residue was crystallized from methanol
출처 및 근거
- ORD 기록
- ord-42e4d6c3b7774f3480a5cd25cb284f3d
- 출처 데이터셋
- uspto-grants-2002_11
- 특허 번호
- US06479536B1
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