反応式
O=P(Cl)(Cl)Cl.[CH3:6][C:7]1[C:13]([OH:14])=[CH:12][CH:11]=[CH:10][C:8]=1[OH:9].[OH-].[Na+].Cl.CN([CH:21]=[O:22])C>O>[OH:9][C:8]1[C:7]([CH3:6])=[C:13]([OH:14])[CH:12]=[CH:11][C:10]=1[CH:21]=[O:22]参加物
実験手順
To an ice-cooled solution of POCl3 (4.9 g, 32.2 mmol) in dry DMF (10.0 mL, 64.4 mmol) was slowly added a solution of 2-methylresorcinol (2.0 g, 16.1 mmol) in dry DMF (5.0 mL). After stirring at room temperature for 12 h, the mixture was cooled to 0° C. and then carefully treated with iced water (15 mL). 2 M sodium hydroxide was added to adjust pH to 10. The resulting mixture was heated to reflux for 10 min. Then, the mixture was acidified by 3 M HCl (pH=3). The resulting solid was collected by filtration, and the precipitate was washed with water (10 mL×3). The obtained orange solid (4.0 g, 46%) was dried in vacuo and used for the next reaction without further purification. 1H-NMR (DMSO-d6, 400 MHz): δ9.71 (1H, s), 7.43 (1H, d, J=8.5 Hz), 6.55 (1H, d, J=8.5 Hz), 1.97 (3H, s).
後処理
- temperaturethe mixture was cooled to 0° C.
- temperatureThe resulting mixture was heated
- temperatureto reflux for 10 min
- filtrationThe resulting solid was collected by filtration
- washthe precipitate was washed with water (10 mL×3)
- dry with materialThe obtained orange solid (4.0 g, 46%) was dried in vacuo
- customused for the next reaction without further purification
出典と根拠
- ORDレコード
- ord-41aea724800a43439c28ab1d42f1a6bb
- 出典データセット
- uspto-grants-2014_10
- 特許番号
- US08865914B2
関連ノート
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