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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 544705Generated: October 30, 2026

Methyl chloroacetate → HCID 20458559, compound

https://huagongshe.com/reaction/544705

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroacetateHCID 7295—
ReactantN-MethyldiallylamineHCID 75501—
SolventAcetoneHCID 180—
ProductHCID 20458559HCID 2045855982.6%

Reaction Steps

To a solution of diallyl methylamine (17.90 g) in acetone (35 ml) was added methyl chloracetate (17.47 g). The mixture was allowed to stand at ambient temperature for 48 hours. The solvent was then removed by evaporation under reduced pressure. The residue, a thick oil, was made more mobile by the addition of isopropanol (5.0 ml) and the product re-precipitated by the addition of ether (700 ml). The product separated as a heavy oil. The ether layer was decanted and the product again mobilised by the addition of isopropanol (5.0 ml). Any residual ether and the isopropanol were removed by evaporation under a vacuum of 1 mmHg and gentle heating. The product N-carbomethoxy methyl-N-methyl-N,N-diallyl ammonium chloride (29.20 g) was isolated as a pale yellow oil (free from starting materials by glc).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04451624
Source datasetuspto-grants-1984_05
ORD IDord-2d0e9bc1adc74dcc8c8f99a221d98c0c
Source noteuspto-grants-1984_05