Sodium Hydroxide → (E)-3-(6-methoxy-3-pentylbenzofuran-2-yl)-2-propenoic acid
반응식
C[O:2][C:3](=[O:22])/[CH:4]=[CH:5]/[C:6]1[O:7][C:8]2[CH:19]=[C:18]([O:20][CH3:21])[CH:17]=[CH:16][C:9]=2[C:10]=1[CH2:11][CH2:12][CH2:13][CH2:14][CH3:15].[OH-].[Na+]>CO>[CH3:21][O:20][C:18]1[CH:17]=[CH:16][C:9]2[C:10]([CH2:11][CH2:12][CH2:13][CH2:14][CH3:15])=[C:6](/[CH:5]=[CH:4]/[C:3]([OH:22])=[O:2])[O:7][C:8]=2[CH:19]=1참가 물질
4
실험 절차
As in Example 112, (E)-3-(6-methoxy-3-pentylbenzofuran-2-yl)-2-propenoic acid methyl ester (4.25 g) in methanol (25 mL) was treated with 2N sodium hydroxide solution (15 mL) at reflux for 1.25 hours. The crude reaction product was crystallized from ethyl acetate to provide 3.6 g of (E)-3-(6-methoxy-3-pentylbenzofuran-2-yl)-2-propenoic acid, mp 146°-147° C. Anal. Calcd for C17H20O4 : C, 70.81; H, 6.99 Found: C, 70.51; H, 6.89
후처리
- temperatureat reflux for 1.25 hours
- customThe crude reaction product
- customwas crystallized from ethyl acetate
출처 및 근거
- ORD 기록
- ord-3550023565dc417f8ed008453e00080e
- 출처 데이터셋
- uspto-grants-1990_05
- 특허 번호
- US04927838
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