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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2055767Generated: November 1, 2026

Carbon Disulfide → HCID 86612043, compound

https://huagongshe.com/reaction/2055767

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DisulfideHCID 6348—
ReactantBromobenzyl CyanideHCID 22044—
ReactantHCID 178418423HCID 178418423—
SolventWaterHCID 962—
ProductHCID 86612043HCID 86612043—

Reaction Steps

To a 100 ml round bottom flask was added 20 ml 2-naphthylmagnesium bromide (0.5M solution in 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 (10:3 mixture of hexane and ethyl ether), pure α-cyanobenzyl dithionaphthalate was obtained as an orange odorless solid (63% yield). Proton and carbon NMR spectra were consistent with the expected structure, CTA-CP-2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07332552B2
Source datasetuspto-grants-2008_02
ORD IDord-6df41bc16a104440a1a018e2575d842b
Source noteuspto-grants-2008_02