Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1734981Generated: October 26, 2026

1-Propanol → O-ethyl O-propyl chlorothiophosphate

https://huagongshe.com/reaction/1734981

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PropanolHCID 1031—
ReactantPhosphorodichloridothioic acid, O-ethyl esterHCID 73907—
Reactant1-Propanol, sodium salt (1:1)HCID 23669363—
SolventTetrahydrofuranHCID 8028—
ProductO-ethyl O-propyl chlorothiophosphateHCID 1252103359.1%

Reaction Steps

To 30 g (167 mmole) of O-ethyl dichlorothiophosphate in 100 ml of tetrahydrofuran (THF) and cooled to -70° C. was added a solution of sodium propoxide (from 7.4 g of 60% NaH (184 mmole) and 11 g (176 mmole) of 1-propanol) in 50 ml of THF. After warming to room temperature over 2 hours, the THF was removed in vacuo and the residue was partitioned between 50 ml diethyl ether, 50 ml hexanes, and 25 ml cold water. The organic layer was dried over magnesium sulfate, concentrated in vacuo, and distilled (bp 45°-50° C. 1 torr) yielding 20 g of the title compound, an oil. nmr 1.0 t 3H, 1.4 t 3H, 1.8 sextet 2H, 4.4M 4H.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05536711
Source datasetuspto-grants-1996_07
ORD IDord-ed45dc17f2de4ca7a18e85bc18e09f7c
Source noteuspto-grants-1996_07