Benzo(B)Thiophene → a-(2-Benzo[b]thienyl)-3,4-(methylenedioxy)benzyl alcohol
반응식
[S:1]1[CH:5]=[CH:4][C:3]2[CH:6]=[CH:7][CH:8]=[CH:9][C:2]1=2.[Li]C(C)(C)C.[CH:15]1[C:20]([CH:21]=[O:22])=[CH:19][C:18]2[O:23][CH2:24][O:25][C:17]=2[CH:16]=1>C1COCC1>[S:1]1[C:5]([CH:21]([OH:22])[C:20]2[CH:15]=[CH:16][C:17]3[O:25][CH2:24][O:23][C:18]=3[CH:19]=2)=[CH:4][C:3]2[CH:6]=[CH:7][CH:8]=[CH:9][C:2]1=2참가 물질
5
실험 절차
α-(2-Benzo[b]thienyl)-3,4-(methylenedioxy)benzyl alcohol was prepared by the method of Example 40A using benzo[b]thiophene (7.5 mmoles, 1.0 g), t-BuLi (1.7 M, 9.7 mmoles, 5.7 ml), piperonal (8.9 mmoles, 1.0 g) and THF (20 ml). Flash chromatography (20% ethyl acetate/hexanes) provided 1.6 g (74%) of a yellow solid.
출처 및 근거
- ORD 기록
- ord-c17bfc1f134841fe9c5f7c6af5923eaf
- 출처 데이터셋
- uspto-grants-2002_01
- 특허 번호
- US06342610B2
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