HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1105579Generated: November 4, 2026
4-Hydroxybenzaldehyde → HCID 53847050, compound
https://huagongshe.com/reaction/1105579
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 20545957 | HCID 20545957 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 53847050 | HCID 53847050 | — |
Reaction Steps
A solution of O-methyl S-ethyl chlorothiophosphate (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 4-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 O-methyl S-ethyl O-(4-formylphenyl) thiophosphate.
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-19703ec9ef1f438b86a5925b1ecfb9ae |
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| Source note | uspto-grants-1982_01 |
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