2-Nitrodibenzofuran → 2-Dibenzofuranamine
反応式
[N+:1]([C:4]1[CH:16]=[CH:15][C:7]2[O:8][C:9]3[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=3[C:6]=2[CH:5]=1)([O-])=O.[H][H]>C(OCC)(=O)C.[Pd]>[NH2:1][C:4]1[CH:16]=[CH:15][C:7]2[O:8][C:9]3[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=3[C:6]=2[CH:5]=1参加物
5
実験手順
In a Parr hydrogenation bottle, 10% Pd/C (0.77 g, 0.724 mmol) was added and the bottle purged with nitrogen. Next 2-nitrodibenzo[b,d]furan (15 g, 44.3 mmol) in 180 mL of ethyl acetate was added and the mixture was hydrogenated on a Parr Hydrogenator until no more hydrogen is taken up by the solution. The catalyst was filtered off through Celite and washed with ethyl acetate. The filtrate was evaporated and pre-absorbed onto Celite. The Celite mixture was purified using a Varian 400 g column eluting with dichloromethane. 10.9 g of product was obtained.
後処理
- customthe bottle purged with nitrogen
- filtrationThe catalyst was filtered off through Celite
- washwashed with ethyl acetate
- customThe filtrate was evaporated
- custompre-absorbed onto Celite
- customThe Celite mixture was purified
- washeluting with dichloromethane
出典と根拠
- ORDレコード
- ord-41852189bc49472cb42b88f3cce2779c
- 出典データセット
- uspto-grants-2015_10
- 特許番号
- US09156870B2
反応ノート
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