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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 3796Generated: October 26, 2026

Cyclohexyl isocyanate → HCID 178418526, compound

https://huagongshe.com/reaction/3796

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexyl isocyanateHCID 18502—
Reactant3-[4-(4-Chlorobenzyl)piperazin-1-yl]propanethiolHCID 13731117—
SolventDichloromethaneHCID 6344—
ProductHCID 178418526HCID 178418526100.7%

Reaction Steps

A mixture of 1.0 g of cyclohexyl isocyanate, 2.1 g of 3-[4-(4-chlorobenzyl)piperazin-1-yl]propanethiol and 10 ml of methylene chloride was stirred at room temperature overnight and then concentrated in vacuo. The residue crystallized upon standing. The product was recrystallized from aqueous ethanol, dissolved in ether, and the ethanol solution was dried (magnesium sulfate). The salt was then precipitated with ethereal hydrochloric acid and recrystallized twice from aqueous ethanol to give 1.2 g (30% of theory) of N-cyclohexyl-S-{3-[4-(4-chlorobenzyl)piperazin-1-yl]propyl}thiocarbamate dihydrochloride as a white crystalline solid, M.p. >165° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04722926
Source datasetuspto-grants-1988_02
ORD IDord-9d1937c896e54cb4b8977e4368ead391
Source noteuspto-grants-1988_02