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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2049339Generated: October 31, 2026

Chloroacetonitrile → HCID 20345057, compound

https://huagongshe.com/reaction/2049339

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetonitrileHCID 7856—
ReactantHCID 23720344HCID 23720344—
ProductHCID 20345057HCID 20345057—

Reaction Steps

The reaction mixture from Example 1 containing potassium p-chlorobenzyl trithiocarbonate is stirred for 0.5 hours and 12.9 ml (200 mmol) of chloroacetonitrile is then added. The temperature of the reaction mixture is adjusted to 20° to 25° C. and stirring is continued for 2 hours. The yellow color from the aqueous layer transfers to the toluene layer and the toluene layer is then separated therefrom, washed with water, brine and dried with Na2SO4. The mixture is filtered and concentrated. The residue is taken up in ether-hexane, reduced in volume and crystallized in a freezer. Recrystallization of this material from ether-hexane gives 28.5 g of p-chlorobenzyl cyanomethyl trithiocarbonate, m.p. 41°-43° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04197311
Source datasetuspto-grants-1980_04
ORD IDord-4844afdf991a4821a6992d85b43ea2de
Source noteuspto-grants-1980_04