Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1657029Generated: October 26, 2026

Hydrochloric Acid → S,N-dimethyl-N'-nitro-N-trichloromethanesulfenylisothiourea

https://huagongshe.com/reaction/1657029

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
ReactantTrichloromethanesulfenyl chlorideHCID 11666—
Reactant1,2-Dimethyl-3-nitroisothioureaHCID 136227017—
SolventDimethylformamideHCID 6228—
ProductS,N-dimethyl-N'-nitro-N-trichloromethanesulfenylisothioureaHCID 7365390657.1%

Reaction Steps

To a cooled, stirred mixture of S,N-dimethyl-N'-nitroisothiourea (1.0 g), triethylamine (0.68 g) and DMF (10 ml) was added 1.2 g of trichloromethanesulfenyl chloride dropwise at 3°-7° C. After stirring at the same temperature for 1 hour, the mixture was poured into 50 ml of 2N hydrochloric acid and the resulting mixture was extracted with toluene (50 ml). The toluene layer was washed with water (50 ml), dried over MgSO4 and concentrated in vacuo. The resulting residue was applied to column chromatography on silica gel. The column was eluted with hexane-AcOEt (8:1). The fractions containing the desired product were concentrated to afford 1.1 g of S,N-dimethyl-N'-nitro-N-trichloromethanesulfenylisothiourea as a pale yellow crystal, m.p. 75°-78° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05256679
Source datasetuspto-grants-1993_10
ORD IDord-341e08c05c364c8098613c4433a8f977
Source noteuspto-grants-1993_10