4-Ethoxy-benzofuran-3-one oxime → 4-Ethoxy-2,3-dihydro-3-benzofuranamine
反応式
[CH2:1]([O:3][C:4]1[C:9]2[C:10](=[N:13]O)[CH2:11][O:12][C:8]=2[CH:7]=[CH:6][CH:5]=1)[CH3:2]>C(O)C.O1CCCC1.[Pd]>[CH2:1]([O:3][C:4]1[C:9]2[CH:10]([NH2:13])[CH2:11][O:12][C:8]=2[CH:7]=[CH:6][CH:5]=1)[CH3:2]参加物
5
実験手順
A mixture of the above described 4-ethoxy-benzofuran-3-one oxime (4.2 g, 21.7 mmol) in ethanol (200 mL) and tetrahydrofuran (200 mL) with 10% palladium on carbon (4.0 g) was hydrogenated at 23° C. and atmospheric pressure for 18 h. Filtered the catalyst off, washed with ethanol, evaporated the filtrate totally and dried in high vacuum to give the title compound as a light brown solid (3.7 g, 1:1 mixture of product and starting material); MS: m/e=163.3 (M+H+).
後処理
- additionA mixture of the
- customwas hydrogenated at 23° C.
- filtrationFiltered the catalyst off,
- washwashed with ethanol
- customevaporated the filtrate totally
- customdried in high vacuum
出典と根拠
- ORDレコード
- ord-a34f9ec0ed704df09f9e253877ae25be
- 出典データセット
- uspto-grants-2012_05
- 特許番号
- US08183380B2
反応ノート
読み込み中…