Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2248194Generated: October 27, 2026

Dimethylamine → S-2-[4-(1-methylpropoxy)phenoxy]ethyl N,N-dimethylthiocarbamate

https://huagongshe.com/reaction/2248194

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
ReactantTriethylamineHCID 8471—
ReactantCarbonyl SulfideHCID 10039—
Reactant2-[4-(1-Methylpropoxy)phenoxy]ethyl bromideHCID 15662590—
Solventtert-ButanolHCID 6386—
ProductS-2-[4-(1-methylpropoxy)phenoxy]ethyl N,N-dimethylthiocarbamateHCID 14552670—

Reaction Steps

Following procedure C in H. Tilles, JACS 81:714 (1959) a solution of dimethylamine (0.58 ml, 8.79 mmol) and triethylamine (1.22 ml, 8.79 mmol) in 3ml of t-butyl alcohol is cooled to 15°, after which carbonylsulfide (0.71 g, 11.87 mmol) is passed in which vigorous stirring. The solution is then warmed to 30°, with stirring, 2-[4-(1-methylpropoxy)phenoxy]ethyl bromide (2.40 g, 8.79 mmol) is added rapidly. The reaction mixture is heated slowly to 50° and maintained at 50° for 3 hours. The solvent is then distilled off and the product is worked up to give S-2-[4-(1-methylpropoxy)phenoxy]ethyl N,N-dimethylthiocarbamate (compound 36, Table B).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05037991
Source datasetuspto-grants-1991_08
ORD IDord-39bc637285114b1d9e5a939404e5d245
Source noteuspto-grants-1991_08