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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 560547Generated: October 31, 2026

Dimethyl N-cyanodithioiminocarbonate → HCID 178512076, compound

https://huagongshe.com/reaction/560547

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl N-cyanodithioiminocarbonateHCID 66289—
ReactantN-BenzylethylenediamineHCID 77801—
SolventDichloromethaneHCID 6344—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178512076HCID 17851207695%

Reaction Steps

To a solution of N-benzylethane-1,2-diamine (3.00 g, 19.96 mmol) in anhydrous dioxane (15 mL) was added dimethyl cyanocarbonimidodithioate (3.50 g, 23.96 mmol). The mixture was refluxed for 16 hours, then diluted with dichloromethane (200 mL), washed with water (200 mL) and brine (100 mL). The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The residue was purified by column chromatography eluted with ethyl acetate/hexane (1/4) to afford the title compound as a colorless solid in 95% yield (3.88 g): mp 120-122° C. (ethyl acetate/hexanes); 1H NMR (300 MHz, CDCl3) δ 7.36-7.22 (m, 5H), 6.86 (br s, 1H), 4.38 (s, 2H), 3.58-3.52 (m, 2H), 3.44-3.88 (m, 2H); 13C NMR (75 MHz, CDCl3) δ 164.0, 135.5, 128.8, 128.1, 127.9, 119.4, 48.3, 46.1, 40.2; MS (ES+) m/z 201.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063084B2
Source datasetuspto-grants-2011_11
ORD IDord-576f64fa42b94289a9c45ddb6c508677
Source noteuspto-grants-2011_11