반응식
[CH3:1][O:2][C:3](=[O:15])[CH2:4][C@H:5]1[C:9]2[CH:10]=[CH:11][C:12]([OH:14])=[CH:13][C:8]=2[O:7][CH2:6]1.[CH2:16]([S:18][CH2:19][CH2:20][O:21][C:22]1[CH:27]=[C:26]([CH3:28])[C:25]([C:29]2[CH:34]=[CH:33][CH:32]=[C:31]([CH2:35]O)[CH:30]=2)=[C:24]([CH3:37])[CH:23]=1)[CH3:17].C(P(CCCC)CCCC)CCC.N(C(N1CCCCC1)=O)=NC(N1CCCCC1)=O>C1(C)C=CC=CC=1.CCCCCC>[CH3:1][O:2][C:3](=[O:15])[CH2:4][C@H:5]1[C:9]2[CH:10]=[CH:11][C:12]([O:14][CH2:35][C:31]3[CH:30]=[C:29]([C:25]4[C:26]([CH3:28])=[CH:27][C:22]([O:21][CH2:20][CH2:19][S:18][CH2:16][CH3:17])=[CH:23][C:24]=4[CH3:37])[CH:34]=[CH:33][CH:32]=3)=[CH:13][C:8]=2[O:7][CH2:6]1참가 물질
7
반응물 4
생성물 1
시약·촉매·용매 2
실험 절차
A solution of methyl[(3S)-6-hydroxy-2,3-dihydro-1-benzofuran-3-yl]acetate (0.250 g, 1.20 mmol), {4′-[2-(ethylthio)ethoxy]-2′,6′-dimethylbiphenyl-3-yl}methanol (0.380 g, 1.20 mmol) and tributylphosphine (0.388 g, 1.92 mmol) in toluene (20 mL) was stirred, 1,1′-(azodicarbonyl)dipiperidine (0.484 g, 1.92 mmol) was added, and the mixture was stirred at room temperature for 1 hr under nitrogen atmosphere. Hexane (10 mL) was added to the reaction mixture, the precipitated insoluble substance was filtered off, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=5:95-40:60) to give the title compound (0.363 g, yield 60%) as a pale-yellow oil.
후처리
- filtrationthe precipitated insoluble substance was filtered off
- concentrationthe filtrate was concentrated under reduced pressure
- customThe residue was purified by silica gel column chromatography (ethyl acetate:hexane=5:95-40:60)
출처 및 근거
- ORD 기록
- ord-3b8d2eeac70e4f3b8da5bb99e838878e
- 출처 데이터셋
- uspto-grants-2010_06
- 특허 번호
- US07732626B2
연결된 노트
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