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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706706Generated: October 25, 2026

Triethylamine hydrochloride → O,O-diethyl N-(chlorothio)-n-propylphosphoramidothioate

https://huagongshe.com/reaction/1706706

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamine hydrochlorideHCID 11130—
ReactantSulfur dichlorideHCID 25353—
ReactantO,O-diethyl propylphosphoramidothioateHCID 2172696—
SolventHexaneHCID 8058—
SolventTriethylamineHCID 8471—
ProductO,O-diethyl N-(chlorothio)-n-propylphosphoramidothioateHCID 20333951—

Reaction Steps

A solution of 2.98 gm. (0.014 mole) O,O-diethyl n-propylphosphoramidothioate in 10 ml. hexane and 2 ml. triethylamine is added to a cold (0° C.) solution of 1.0 ml. (0.016 mole) sulfur dichloride in 10 ml. hexane slowly and with stirring. There is vigorous reaction and heavy precipitation of triethylamine hydrochloride. An additional 20 ml. hexane is added. The reaction mixture is kept at 0° to 5° C. and stirred for 30 minutes, then it is filtered. The filtrate is concentrated to a pale yellow oil by evaporating the hexane under reduced pressure. The oil comprises the desired O,O-diethyl N-(chlorothio)-n-propylphosphoramidothioate which can be used for further reactions with N-methylcarbamates.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04208409
Source datasetuspto-grants-1980_06
ORD IDord-eb62bfc35fec4a00bf1f1371c41c0480
Source noteuspto-grants-1980_06