HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1731564Generated: October 25, 2026
Triphenylphosphine → Acetic acid, 2-(triphenylphosphoranylidene)-, methyl ester
https://huagongshe.com/reaction/1731564
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methyl bromoacetate | HCID 60984 | — |
| Reactant | Phosphonium, (2-methoxy-2-oxoethyl)triphenyl-, bromide (1:1) | HCID 2733211 | — |
| Reactant | Phosphonium | HCID 5460504 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Water | HCID 962 | — |
| Product | Acetic acid, 2-(triphenylphosphoranylidene)-, methyl ester | HCID 17453 | 80% |
Reaction Steps
Triphenyl phosphine (13 g.) was dissolved in dry benzene (60 ml.) and methyl bromoacetate (8.3 g.) was added dropwise. The solution was heated at 70° C., for 2 days, and then cooled and filtered. The residue was washed with benzene and dried to give about 16 g. of (methoxycarbonyl methyl)triphenylphosphonium bromide. The phosphonium salt (10 g.) was dissolved in water (250 ml.) and 5% aqueous sodium hydroxide was added dropwise with stirring until the solution became alkaline to litmus. The resulting precipitate was filtered off, washed with water and dried. Crystallisation from ethyl acetate/petroleum spirit gave (methoxycarbonyl methylene) triphenyl phosphorane as a colourless solid in about 80% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04622337 |
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| Source dataset | uspto-grants-1986_11 |
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| ORD ID | ord-3476553ebdfe4c05b6d48784eacaf486 |
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| Source note | uspto-grants-1986_11 |
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