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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 335350Generated: October 30, 2026

Carbon Disulfide → HCID 17866105, compound

https://huagongshe.com/reaction/335350

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DisulfideHCID 6348—
ReactantBromobenzeneHCID 7961—
Reactantp-Vinylbenzyl chlorideHCID 74126—
ProductHCID 17866105HCID 17866105—
ProductHCID 86654443HCID 86654443—

Reaction Conditions

Temperature50 °C

Reaction Steps

4-vinylbenzyl dithiobenzoate (VBThB) was prepared according to reaction scheme 4, as follows. A 500 mL round bottom flask was dried with 3 vacuum/heat/nitrogen cycles. 100 mL of dry THF was added along with 3.3 grams of magnesium turnings. The mixture was placed in an oil bath set to 40° C., and 13.8 grams (0.088 moles) bromobenzene was added. 7.91 mL (0.088 moles) of dry carbon disulfide was added dropwise over the next 15 minutes. When all the carbon disulfide was added, the temperature was increased to 50° C., and 18.62 grams (0.088 moles) of 4-vinylbenzyl chloride was added. The solvent was removed. The crude product was purified via column chromatography over activated alumina (Brockman activity II). The final product was obtained as a red oil. The conversion was estimated at 48% after eluent removal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883912B2
Source datasetuspto-grants-2014_11
ORD IDord-63aa2bfd23c04708b1f47e88d539f1a5
Source noteuspto-grants-2014_11