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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2055770Generated: October 31, 2026

Bromide ion → HCID 58856298, compound

https://huagongshe.com/reaction/2055770

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromide ionHCID 259—
ReactantWaterHCID 962—
ReactantCarbon DisulfideHCID 6348—
ReactantBromobenzyl CyanideHCID 22044—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58856298HCID 58856298—

Reaction Steps

To a 100 ml round bottom flask was added 10 ml 4-tolylmagiesium bromide (1.0M solution in ethyl ether) and diluted to 20 ml with anhydrous THF. 0.76 g carbon disulfide was added dropwise to this mixture and stirred for ½ h at room temperature. Then to the dark red solution was added 2 g α-bromobenzeneacetonitrile dropwise and the mixture stirred for another 2 h. Water was added to the mixture and the organic product was extracted with diethyl ether (3×50 ml), dried with magnesium sulfate overnight and filtered. After removal of solvent and column chromatography (5:2 mixture of hexane and ethyl ether), pure α-cyanobenzyl 4-methyldithiobenzoate was obtained as a red odorless solid (48% yield). Proton and carbon NMR spectra were consistent with the expected structure, CTA-CP-6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07332552B2
Source datasetuspto-grants-2008_02
ORD IDord-418b1d1043f64bbeaf437f1b066bce05
Source noteuspto-grants-2008_02