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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1105587Generated: October 27, 2026

Salicylaldehyde → S-Ethyl S-Propyl O-(2-Formylphenyl) Trithiophosphate

https://huagongshe.com/reaction/1105587

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSalicylaldehydeHCID 6998—
ReactantTriethylamineHCID 8471—
ReactantS-ethyl S-propyl chlorotrithiophosphateHCID 57142200—
SolventDichloromethaneHCID 6344—
ProductS-Ethyl S-Propyl O-(2-Formylphenyl) TrithiophosphateHCID 57137846—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of S-ethyl S-propyl chlorotrithiophosphate (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 2-hydroxybenzaldehyde (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-propyl O-(2-formylphenyl)trithiophosphate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04309422
Source datasetuspto-grants-1982_01
ORD IDord-8081d7d64a0c47b69aa32cca630b553a
Source noteuspto-grants-1982_01