反応式
[O:1]([CH2:8][CH2:9][C:10]([OH:12])=[O:11])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.O=S(Cl)Cl.[CH3:17]O>>[O:1]([CH2:8][CH2:9][C:10]([O:12][CH3:17])=[O:11])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1参加物
4
反応条件
- 温度
- 0 °C
実験手順
3-Phenoxypropionic acid (10.0 g, 60 mmol) was dissolved in methanol (100 mL). The reaction mixture was allowed to cool to 0° C. and SOCl2 was slowly added over a 15 min period. The reaction mixture was slowly allowed to warm to room temperature over a 2 h period. The reaction mixture was concentrated in vacuo, then redissolved in ethyl acetate (100 mL). The organic layer was washed with water (2×150 mL), dried (MgSO4), concentrated in vacuo to provide crude product in 95% yield. 1H NMR (CDCl3)δ2.84 (t, J=6.4 Hz, 2H), 3.76 (s, 3H), 4.28 (t, J=6.4 Hz, 2H), 6.95 (m, 3H), 7.31 (m, 2H).
後処理
- temperatureto warm to room temperature over a 2 h period
- concentrationThe reaction mixture was concentrated in vacuo
- dissolutionredissolved in ethyl acetate (100 mL)
- washThe organic layer was washed with water (2×150 mL)
- dry with materialdried (MgSO4)
- concentrationconcentrated in vacuo
- customto provide crude product in 95% yield
出典と根拠
- ORDレコード
- ord-483405582b68479092df9ac35b3d658d
- 出典データセット
- uspto-grants-2003_07
- 特許番号
- US06586437B2
関連ノート
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