反応式
[C:1]([O:7][CH2:8][CH3:9])(=[O:6])[CH2:2][C:3]([CH3:5])=O.P(Cl)(Cl)(Cl)(Cl)[Cl:11]>O>[CH2:8]([O:7][C:1](=[O:6])[CH:2]=[C:3]([Cl:11])[CH3:5])[CH3:9]参加物
反応条件
- 温度
- 25 °C
実験手順
To a stirred mixture of ethyl acetoacetate (15.0 g, 0.12 mol) in petroleum ether (30 mL) under a nitrogen atmosphere was added phosphorus pentachloride (12.7 g, 0.06 mol) gradually. After addition was complete the mixture was stirred at 25° C. for 1 h. Upon completion of the reaction water (50 mL) was added in small portions, transferred to a separatory funnel and the layers separated, followed by washing the aqueous layer with petroleum ether (2×50 mL). The combined petroleum ether extracts were washed with a 20% potassium carbonate solution, followed by a saturated sodium chloride solution and dried over magnesium sulfate. The combined organic layers were concentrated to give a yellow oil. Distillation of the residue yielded 3-chloro-but-2-enoic acid ethyl ester (7.4 g 43%) as a clear oil: LR-ES-MS m/z calculated for C6H9ClO2 [M]+ 148, observed [M+H]+ 149.
後処理
- additionAfter addition
- additionwas added in small portions
- customtransferred to a separatory funnel
- customthe layers separated
- washby washing the aqueous layer with petroleum ether (2×50 mL)
- washThe combined petroleum ether extracts were washed with a 20% potassium carbonate solution
- dry with materialdried over magnesium sulfate
- concentrationThe combined organic layers were concentrated
- customto give a yellow oil
- distillationDistillation of the residue
出典と根拠
- ORDレコード
- ord-e6036ef11aa9408e8fa664960532b4d3
- 出典データセット
- uspto-grants-2010_06
- 特許番号
- US07741327B2
関連ノート
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