Hydrochloric Acid → N-(2-fluoroethyl)-N-methyloxamic acid
反応式
[CH3:1]O.[OH-].[Na+].Cl.[F:6][CH2:7][CH2:8][N:9](NC)[C:10](=[O:14])[C:11]([OH:13])=[O:12]>O>[F:6][CH2:7][CH2:8][N:9]([CH3:1])[C:10](=[O:14])[C:11]([OH:13])=[O:12]参加物
6
実験手順
To a mixed solvent comprising 6 ml of methanol and 5 ml of water, there was suspended 1.56 g of N-(2-fluoroethyl)-N-methylmethoxyoxalylamide, then 3.2 g of a 15% aqueous solution of sodium hydroxide was dropwise added, with ice-cooling, to the suspension and then the mixture was stirred for one hour. Concentrated hydrochloric acid was added to the reaction system, the mixture was then extracted with ethyl acetate, the organic phase thus separated was washed with water, dried over magnesium sulfate and then the ethyl acetate was distilled off from the organic phase to thus give, as the target product, 0.94 g (yield: 66%, a solid product) of N-(2-fluoroethyl)-N-methylaminooxamic acid.
後処理
- temperaturecooling, to the suspension
- extractionthe mixture was then extracted with ethyl acetate
- customthe organic phase thus separated
- washwas washed with water
- dry with materialdried over magnesium sulfate
- distillationthe ethyl acetate was distilled off from the organic phase
- customto thus give, as the target product, 0.94 g (yield: 66%
出典と根拠
- ORDレコード
- ord-d44f2c5488034fda8a8f1830b69e4112
- 出典データセット
- uspto-grants-2013_09
- 特許番号
- US08541473B2
反応ノート
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