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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 918042Generated: October 30, 2026

Benzenesulfenyl chloride → 1-Methyl-2-[nitro(phenylsulfanyl)methylidene]imidazolidine

https://huagongshe.com/reaction/918042

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfenyl chlorideHCID 11008040—
Reactant1-Methyl-2-(nitromethylidene)imidazolidineHCID 70250046—
SolventPyridineHCID 1049—
Product1-Methyl-2-[nitro(phenylsulfanyl)methylidene]imidazolidineHCID 70639009—

Reaction Steps

14.6 g of phenylsulfenyl chloride was added dropwise to a cooled, stirred solution of 14.3 g of Compound 1 in 250 ml of pyridine. The mixture was allowed to stand overnight at room temperature, then excess pyridine was recovered on a rotary evaporator. The residue was treated with 250 ml of water and the mixture extracted with methylene chloride. The combined extracts were dried and the solvent evaporated to give a crystalline solid which was triturated with ethyl acetate, then ethanol, to yield 25, as a yellow solid, melting point: 170° - 173°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03969354
Source datasetuspto-grants-1976_07
ORD IDord-55756baa408e4d72b2cff268dee583fb
Source noteuspto-grants-1976_07