HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 259206Generated: October 29, 2026
Triphenylphosphine → 3-Ethoxypropionylmethylenetriphenylphosphorane
https://huagongshe.com/reaction/259206
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 1-Chloro-4-ethoxybutan-2-one | HCID 14068889 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 3-Ethoxypropionylmethylenetriphenylphosphorane | HCID 20542922 | 53.3% |
Reaction Steps
A solution of 1-chloro-4-ethoxybutan-2-one (7.5 g.) and triphenylphosphine (13.5 g.) in chloroform (20 ml.) was saturated with nitrogen and heated at reflux under nitrogen overnight. The chloroform was removed in vacuo and the residue was dissolved in dichloromethane (35 ml.). Dry diethyl ether (300 ml.) was added to precipitate 4-ethoxy-2-oxobutyltriphenylphosphonium chloride (19 g.). This compound was added portionwise to a solution of sodium carbonate (10g.) in water (1000 ml.) and the mixture was stirred vigorously for 24 hours. The solution was extracted with diethyl ether, and the ethereal extracts were dried over magnesium sulphate. The solvent was removed by evaporation and the residue was cooled and triturated with petroleum ether (b.p. 60°-80° C.) to give 3-ethoxypropionylmethylenetriphenylphosphorane (10.0 g.), m.p. 63°-65° C. Elemental analysis: found C, 76.6; H, 6.5; P, 8.2%; C24H25O2P requires: C, 76.6; H, 6.7;P 8.3%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04036872 |
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| Source dataset | uspto-grants-1977_07 |
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| ORD ID | ord-8c5d8aed142748ad959f05a6a779aefe |
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| Source note | uspto-grants-1977_07 |
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