Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1898801Generated: October 26, 2026

Benzyl Chloride → HCID 178429177, compound

https://huagongshe.com/reaction/1898801

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl ChlorideHCID 7503—
ReactantTriethylamineHCID 8471—
ReactantThiosemicarbazideHCID 2723789—
ReactantSodium MethoxideHCID 10942334—
Reactant4-Methylglutaconic anhydrideHCID 22086937—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
SolventIsopropanolHCID 3776—
SolventEthyl AcetateHCID 8857—
ProductHCID 178429177HCID 178429177—

Reaction Steps

A mixture of thiosemicarbazide (50.0 g, 0.554 mol) and benzyl chloride (67.1 g, 0.53 mol) in 2-propanol (1 L) was heated to reflux with stirring for 2 hours. The reaction mixture was then cooled and 4-methylglutaconic anhydride (60.8 g, 0.482 mol) and triethylamine (75 mL, 53.6 g, 0.53 mol) were added. The reaction mixture was again heated at reflux with stirring for an hour. Sodium methoxide in methanol solution (250 mL of 25 percent, 1.09 mol) was then added and the yellow-brown mixture obtained was heated at reflux with stirring for 2.5 hours. The volatiles were removed by evaporation under reduced pressure and the residue obtained was combined with dilute aqueous acetic acid (150 mL) and ethyl acetate. The organic phase was recovered, washed well with water and concentrated by evaporation under reduced pressure. The residue obtained was heated with a heat gun under reduced pressure for 30 minutes until the bubbling had stopped and the reaction mixture had solidified. The mixture was cooled and diluted with methanol and the resulting solids were recovered by filtration to obtain 54.5 g (41 percent of theory) of the title compound as a yellow-brown powder melting at 214°-216° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05571775
Source datasetuspto-grants-1996_11
ORD IDord-71f8151f30e4426987390ad6bb5aac87
Source noteuspto-grants-1996_11