反応式
[CH3:1][O:2][C:3]1[CH:13]=[C:12]([C:14]#[N:15])[CH:11]=[CH:10][C:4]=1[O:5][CH2:6][C:7]([OH:9])=[O:8].N>[Ni].CO>[CH3:1][O:2][C:3]1[CH:13]=[C:12]([CH2:14][NH2:15])[CH:11]=[CH:10][C:4]=1[O:5][CH2:6][C:7]([OH:9])=[O:8]参加物
5
実験手順
3.3 g of 2-(2-methoxy-4-cyanophenoxy)-acetic acid are hydrogenated in 90 ml of a 2:1 (by volume) mixture of methanol and 25% aqueous ammonia in the presence of 1.6 g of Raney nickel for 5 hours at room temperature under normal pressure. After filtering off the catalyst, it is washed with methanol and water and the filtrate is then concentrated to dryness. The resulting solid material is triturated with a small amount of water, filtered off and dried over P2O5 in an exsiccator.
後処理
- filtrationAfter filtering off the catalyst, it
- washis washed with methanol and water
- concentrationthe filtrate is then concentrated to dryness
- customThe resulting solid material is triturated with a small amount of water
- filtrationfiltered off
- dry with materialdried over P2O5 in an exsiccator
出典と根拠
- ORDレコード
- ord-5c964da8f7d04622a287b1ab22922095
- 出典データセット
- uspto-grants-1990_10
- 特許番号
- US04965260
関連ノート
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