Methanol → 2-(1H-1,2,4-triazol-3-yl)acetic acid
反応式
[NH:1]1[CH:5]=[N:4][C:3]([CH2:6][C:7]([O:9]CC)=[O:8])=[N:2]1.[OH-].[Na+].O.CO>C1COCC1>[NH:1]1[CH:5]=[N:4][C:3]([CH2:6][C:7]([OH:9])=[O:8])=[N:2]1参加物
6
反応条件
- 温度
- 100 °C
実験手順
A mixture of ethyl 1H-1,2,4-triazol-3-ylacetate obtained in Reference Example 14 (900 mg, 5.80 mmol), 4N aqueous sodium hydroxide solution (7.25 mL, 29.0 mmol), water (10 mL), methanol (10 mL) and THF (10 mL) was stirred at 100° C. for 2 hr. The reaction mixture was concentrated under reduced pressure, the residue was acidified with 1N hydrochloric acid, and the mixture was concentrated under reduced pressure. Ethanol was added to the residue, and the insoluble material was filtered off, and the filtrate was concentrated. The residue was crystallized from toluene to give the title compound as a white powder (369 mg, 50%).
後処理
- concentrationThe reaction mixture was concentrated under reduced pressure
- concentrationthe mixture was concentrated under reduced pressure
- additionEthanol was added to the residue
- filtrationthe insoluble material was filtered off
- concentrationthe filtrate was concentrated
- customThe residue was crystallized from toluene
出典と根拠
- ORDレコード
- ord-ec4c4f925dda47fb8817c9f10dff6bc8
- 出典データセット
- uspto-grants-2011_03
- 特許番号
- US07915267B2
反応ノート
読み込み中…