Methanol → 2-Methyl-3-oxo-3-(phenylamino)propanoic acid
反応式
[CH3:1][CH:2]([C:8](=[O:16])[NH:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)[C:3]([O:5]CC)=[O:4].[OH-].[Na+].O.CO>C1COCC1>[CH3:1][CH:2]([C:8](=[O:16])[NH:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)[C:3]([OH:5])=[O:4]参加物
6
実験手順
Prepared according to Procedure B using ethyl 2-methyl-3-oxo-3-(phenylamino)-propanoate (8.60 g, 39 mmol) and sodium hydroxide (2.00 g, 50 mmol) in THF (40.00 mL), water (10.00 mL, 555 mmol) and MeOH (10.00 mL) to afford product as a colorless solid, which was used without further purification. Mass Spectrum (ESI) m/e=192.1 [M−1].
後処理
- customPrepared
- customto afford product as a colorless solid, which
- customwas used without further purification
出典と根拠
- ORDレコード
- ord-00730ec492f948fd8708dd1610a637d8
- 出典データセット
- uspto-grants-2015_01
- 特許番号
- US08940724B2
反応ノート
読み込み中…