HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1452432Generated: October 25, 2026
Allyl Alcohol → Allyl P,P-diethylphosphonoacetate
https://huagongshe.com/reaction/1452432
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Allyl Alcohol | HCID 7858 | — |
| Reactant | (Diethoxyphosphinyl)acetic acid | HCID 36704 | — |
| Reactant | N-(3-methylaminopropyl)-N'-ethylcarbodiimide hydrochloride | HCID 9794023 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Allyl P,P-diethylphosphonoacetate | HCID 4583084 | 82.2% |
Reaction Steps
29.2 g of the diethylphosphonoacetic acid thus obtained was dissolved in 350 ml of methylene chloride, and 17.8 g of allyl alcohol, 1.92 g of 4-dimethylaminopyridine and 29.0 g of 1-ethyl-3-(3-methylaminopropyl)carbodiimide hydrochloride were added thereto with stirring under cooling with ice. The mixture was stirred at room temperature overnight. The reaction solution was evaporated under reduced pressure. The residue was dissolved in ethyl acetate, then sequentially washed with 1N hydrochloric acid, water, a saturated sodium hydrogencarbonate aqueous solution and a saturated sodium chloride aqueous solution, and dried over anhydrous magnesium sulfate. The drying agent was separated by filtration, and then the solvent was distilled off under reduced pressure to obtain 28.9 g of allyl diethylphosphonoacetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05606101 |
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| Source dataset | uspto-grants-1997_02 |
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| ORD ID | ord-76f15d3f7acd412ba981e865e2ec841a |
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| Source note | uspto-grants-1997_02 |
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