Hydrochloric Acid → 2-(2-Aminothiazole-4-yl)-2-methoxyiminoacetic acid
反応式
[CH3:1][O:2][N:3]=[C:4]([C:10]1[N:11]=[C:12]([NH2:15])[S:13][CH:14]=1)[C:5]([O:7]CC)=[O:6].[OH-].[Na+].Cl>C(O)C>[CH3:1][O:2][N:3]=[C:4]([C:10]1[N:11]=[C:12]([NH2:15])[S:13][CH:14]=1)[C:5]([OH:7])=[O:6]参加物
実験手順
Ethanol (10 ml.) was added to a suspension of ethyl 2-methoxyimino-2-(2-aminothiazol-4-yl)acetate (syn isomer), which can be represented as ethyl 2-methoxyimino-2-(2-imino-2,3-dihydrothiazol-4-yl)acetate (syn isomer), (2.2 g.) in a 1 N aqueous solution of sodium hydroxide (12 ml.) and the mixture was stirred for 15 hours at ambient temperature. The reaction mixture was adjusted to pH 7.0 with 10% hydrochloric acid and ethanol was distilled off under reduced pressure. The residual aqueous solution was washed with ethyl acetate, adjusted to pH 2.8 with 10% hydrochloric acid and stirred under ice-cooling to precipitate crystals. The crystals were collected by filtration, washed with acetone and recrystallized from ethanol to give colorless needles of 2-methoxyimino-2-(2-aminothiazol-4-yl)acetic acid (syn isomer), which can be represented as 2-methoxyimino-2-(2-imino-2,3-dihydrothiazol-4-yl)acetic acid (syn isomer), (1.1 g.).
後処理
- distillationwas distilled off under reduced pressure
- washThe residual aqueous solution was washed with ethyl acetate
- stirringstirred under ice-
- temperaturecooling
- customto precipitate crystals
- filtrationThe crystals were collected by filtration
- washwashed with acetone
- customrecrystallized from ethanol
出典と根拠
- ORDレコード
- ord-560b09e0caa84bf1a197f81caf390cf5
- 出典データセット
- uspto-grants-1980_09
- 特許番号
- US04225707
反応ノート
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