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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 344970Generated: October 30, 2026

Carbon Disulfide → HCID 178441374, compound

https://huagongshe.com/reaction/344970

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DisulfideHCID 6348—
ReactantBenzyl ChlorideHCID 7503—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 12801340HCID 12801340—
SolventWaterHCID 962—
ProductHCID 178441374HCID 178441374—

Reaction Steps

28.6 g (0.2 mole) of 2-methyl-2-(tert.butyl)-oxazolidine and 8.0 g (0.2 mole) of sodium hydroxide dissolved in 80 cm3 of water were placed into a round-bottom flask equipped with a reflux condenser, a thermometer, a dropping funnel and a stirrer. With continuous stirring and cooling, 15.2 g (12.05 cm3, 0.2 mole) of carbon disulphide was introduced dropwise while the temperature was not allowed to rise above 20° C. As the introduction of carbon disulphide had been completed, the mixture was continued to stir at room temperature for 2 hours. Under cooling and stirring, 25.2 g (22.96 cm3, 0.2 mole) of benzylchloride was added dropwise below 10° C. Stirring was continued for 2 hours after the introduction had been completed. The organic layer was separated from the aqueous one and the latter was extracted by chloroform. The unified organic phases were washed with water, dried above sodium sulphate, and then the solvent was distilled off. Yield: 36.8 g (61.8%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05055125
Source datasetuspto-grants-1991_10
ORD IDord-2ffc6c6550e247fbab32d192c3c2238a
Source noteuspto-grants-1991_10