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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 841052Generated: October 30, 2026

Bromine → Hydrogen Bromide

https://huagongshe.com/reaction/841052

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantBenzyl (2-chloroprop-2-en-1-yl)carbamodithioateHCID 54395229—
SolventEthyl AcetateHCID 8857—
ProductHydrogen BromideHCID 260—
ProductHCID 23450655HCID 23450655—

Reaction Conditions

Temperature0.5 °C

Reaction Steps

Under a slight stream of nitrogen, 19.9 g of (2-chloro-allyl)-dithiocarbamic acid benzyl ester are placed in 100 ml of ethyl acetate and cooled to 0-1° C. During the addition of bromine, the apparatus is flushed thoroughly with nitrogen. 14.0 g of bromine are added in the course of 40 minutes in such a manner that the temperature can be maintained at 0-10° C. When the addition is complete, stirring is carried out for about 20 minutes. The reaction mixture is concentrated in vacuo at 20-250C. 50 ml of hexane are added, the mixture is filtered at 20-25° C., and the filtration residue is washed with 40 ml of hexane and dried in vacuo at room temperature. The title product is obtained in the form of the hydrobromide (compound 2.1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06369233B1
Source datasetuspto-grants-2002_04
ORD IDord-1efd337d0ebc4865b1881b0d13f9f6f3
Source noteuspto-grants-2002_04