Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1105584Generated: October 26, 2026

Triethylamine → S-ethyl S-hexyl O-(3-formylmethylphenyl) dithiophosphate

https://huagongshe.com/reaction/1105584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-(3-Hydroxyphenyl)acetaldehydeHCID 14995207—
ReactantS-ethyl S-hexyl chlorodithiophosphateHCID 86738193—
SolventDichloromethaneHCID 6344—
ProductS-ethyl S-hexyl O-(3-formylmethylphenyl) dithiophosphateHCID 86738192—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of S-ethyl S-hexyl chlorodithiophosphate (0.03 mole) in methylene chloride (50 ml) is charged into a glass reaction vessel equipped with a mechanical stirrer. Triethylamine (0.03 mole) is added and the mixture is cooled to a temperature of about 0° C. A solution of 3-hydroxylphenylacetaldehyde (0.03 mole) in methylene chloride (15 ml) is slowly added with stirring while maintaining the temperature of the reaction mixture at about 0° C. After the addition is completed, the reaction mixture is allowed to warm to room temperature and stirring is continued for a period of about 1 hour. After this time the reaction mixture is transferred to a separatory funnel and methylene chloride (100 ml) is added. The resulting solution is then washed with water, dilute aqueous sodium hydroxide and again with water. The washed solution is dried over anhydrous magnesium sulfate, is filtered and stripped of solvent under vacuum to yield the desired product S-ethyl S-hexyl O-(3-formylmethylphenyl) dithiophosphate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04309422
Source datasetuspto-grants-1982_01
ORD IDord-cd5744d3d2aa44afb5c5def9cfb78ba6
Source noteuspto-grants-1982_01