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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-(3-Hydroxyphenyl)acetaldehyde | HCID 14995207 | — |
| Reactant | S-ethyl S-hexyl chlorodithiophosphate | HCID 86738193 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | S-ethyl S-hexyl O-(3-formylmethylphenyl) dithiophosphate | HCID 86738192 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04309422 |
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| Source dataset | uspto-grants-1982_01 |
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| ORD ID | ord-cd5744d3d2aa44afb5c5def9cfb78ba6 |
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| Source note | uspto-grants-1982_01 |
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