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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2290853Generated: October 27, 2026

Cyclohexyl isocyanate → HCID 178418526, compound

https://huagongshe.com/reaction/2290853

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 numberUS04618677
Source datasetuspto-grants-1986_10
ORD IDord-73fb518343bf46899514354c659c4b0d
Source noteuspto-grants-1986_10