Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1779903Generated: October 25, 2026

Acetic Acid → 2-Bromobenzylidene diethylmalonic acid

https://huagongshe.com/reaction/1779903

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPiperidineHCID 8082—
Reactant2-BromobenzaldehydeHCID 81129—
ReactantDiethylmaloic acidHCID 21642744—
SolventBenzeneHCID 241—
SolventDiethyl EtherHCID 3283—
Product2-Bromobenzylidene diethylmalonic acidHCID 6708464590%

Reaction Steps

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%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05629254
Source datasetuspto-grants-1997_05
ORD IDord-cb9a63dca1a448c2adcb5d0f861846c5
Source noteuspto-grants-1997_05