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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2073128Generated: November 1, 2026

Methyl chloroformate → 5-Butyl-2-(4-isothiocyanatophenyl)pyrimidine

https://huagongshe.com/reaction/2073128

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroformateHCID 6586—
ReactantHCID 22152660HCID 22152660—
SolventChloroformHCID 6212—
SolventTriethylamineHCID 8471—
Product5-Butyl-2-(4-isothiocyanatophenyl)pyrimidineHCID 1461895081%

Reaction Steps

6.77 g of triethylammonium p-(5-butyl-2-pyrimidinyl)phenyldithiocarbamate were largely dissolved in 60 ml of chloroform and 2.5 ml of triethylamine. The mixture was subsequently treated dropwise with 2.00 ml of methyl chloroformate within 5 minutes while stirring and cooling with an ice bath. The ice bath was removed after 10 minutes. After a further 60 minutes the yellowish solution was washed once with 20 ml of 0.5N hydrochloric acid and three times with 20 ml of water each time, dried over sodium sulphate and concentrated. Chromatography of the residue on 60 g of silica gel with hexane/ethyl acetate (vol. 95:5) gave 3.65 g of p-(5-butyl-2-pyrimidinyl)phenyl isothiocyanate which was recrystallized twice from hexane for further purification. Yield 3.17 g; m.p. (C--S) 60.8° C., cl.p. (S--I) 77.8° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04915480
Source datasetuspto-grants-1990_04
ORD IDord-8044d42b70e94eb986cc1270ff4db333
Source noteuspto-grants-1990_04