反应 #1357

反应方程式

2-bromobenzaldehyde

diethylmaloic acid

piperidine

acetic acid

→

desired product

收率 90.0%

2-bromobenzylidene diethylmalonic acid

收率 90.0%

溶剂

benzene

ether

反应条件

后处理

1. 1
   其他A 500-ml three-necked round flask (Dean & Stark) equipped with a stirring bar
2. 2
   洗涤by washing with 100 ml of water two times
3. 3
   干燥The organic phase was dried over anhydrous Na2SO4
4. 4
   浓缩The solvent was concentrated under reduced pressure
5. 5
   浓缩the concentrate of a orange liquid
6. 6
   workup.DISTILLATIONwas distilled under reduced pressure

实验过程

A 500-ml three-necked round flask (Dean & Stark) equipped with a stirring bar, a Dimroth condenser and a thermometer was charged with 74.0 g (400 mmol) of 2-bromobenzaldehyde, 70.48 g (440 mmol) of diethylmaloic acid, 1.6 ml of piperidine, 4.8 ml of acetic acid and 80 ml of benzene. The mixture was subjected to azeotoropic dehydration for 7 hours in an oil bath of 110° C. under a nitrogen atmosphere. After the reaction was completed, the reaction mixture was cooled to room temperature and 300 ml of ether was added, followed by washing with 100 ml of water two times. The organic phase was dried over anhydrous Na2SO4. The solvent was concentrated under reduced pressure and the concentrate of a orange liquid was distilled under reduced pressure to obtain 117.2 g of the desired product as a yellow liquid (yield: 90%).

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