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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1461767Generated: November 1, 2026

Carbon Disulfide → HCID 19979372, compound

https://huagongshe.com/reaction/1461767

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DisulfideHCID 6348—
ReactantTriethylamineHCID 8471—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantHCID 19979371HCID 19979371—
SolventPyridineHCID 1049—
ProductHCID 19979372HCID 19979372—

Reaction Conditions

Temperature-10 °C

Reaction Steps

A solution of 5.0 g of triethylamine in 10 ml of pyridine is cooled to from -5° C. to -10° C., and 20 ml of carbon disulfide are added dropwise. At -10° C., a solution of 15.0 g of 2,4-diisopropyl-6-(4-chlorophenoxy)-3-aminopyridine in 27 ml of pyridine is slowly added dropwise. The mixture is further stirred at -10° C. for 1 hour. A solution of 10.0 g of N,N'-dicyclohexylcarbodiimide in 10 ml of pyridine is then added. After a further 3 hours at -10° C., the mixture is stirred for 18 hours at room temperature. The reaction mixture is concentrated by evaporation and hexane is added to the residue. Thehhexane solution is filtered off and concentrated by evaporation. 2,4-Diisopropyl-6-(4-chlorophenoxy)-pyrid-3-yl isothiocyanate is obtained in the form of a yellow oil, which is used for the next reaction without being further purified; IR (CCl 4): 2090, 1490, 1220 cm-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05077304
Source datasetuspto-grants-1991_12
ORD IDord-7a5ca98f2e1141928f89b024ff66ffcb
Source noteuspto-grants-1991_12