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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1700836Generated: October 26, 2026

Allyl chloride → Diallyl malonate

https://huagongshe.com/reaction/1700836

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl chlorideHCID 7850—
ReactantChlorobenzeneHCID 7964—
ReactantMalonic acid, disodium saltHCID 8865—
CatalystTetrabutylammonium BromideHCID 74236—
SolventWaterHCID 962—
ProductDiallyl malonateHCID 22822716%

Reaction Conditions

Temperature100 °C

Reaction Steps

In an autoclave, 7.65 g (0.1 mol) of allyl chloride were added to a solution of 2.96 g (20 mmol) of disodium malonate and 0.64 g (2 mmol) of tetrabutylammonium bromide in 5 ml of water and 10 ml of chlorobenzene. The mixture was heated to 100° C. over a period of 30 minutes, with the pressure in the autoclave rising to 2.5 bar. After a reaction time of 3½ hours at 100° C., the mixture was cooled to room temperature and depressurized. The aqueous phase was extracted with tert-butyl methyl ether (2×5 ml). The combined organic phases were dried over sodium sulfate and analyzed by gas chromatography (internal standard: dimethyl succinate). The product yield was 16 percent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06350898B1
Source datasetuspto-grants-2002_02
ORD IDord-b57fe02393d84ac1b47f8c7cdcf0b734
Source noteuspto-grants-2002_02