HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1265173Generated: October 26, 2026
Triphenylphosphine → 3-Oxo-cyclopentanecarboxylic acid methyl ester
https://huagongshe.com/reaction/1265173
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Ozone | HCID 24823 | — |
| Reactant | Methyl 3-methylidenecyclopentane-1-carboxylate | HCID 557110 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Oxo-cyclopentanecarboxylic acid methyl ester | HCID 237640 | 54% |
Reaction Steps
A solution of methyl 3-methylenecyclopentane carboxylate (Trost, B. M., Chan, M. T., J. Am. Chem. Soc., 1983, 105, 2315) (2.84 g, 20.26 mmol) in dichloromethane (60 mL) was cooled to −78° C. and a slow stream of ozone was passed through until the permanent blue color indicated complete ozonide formation. The excess ozone was purged with stream of nitrogen. Triphenylphosphine (10.62 g, 40.52 mmol) was added, and stirring was continued overnight, allowing the temperature to warm up to ambient. Solvent was removed in vacuo, the residue dissolved in 10 mL of ethyl acetate/hexane (1:4) mixture. The crystalline triphenylphosphine oxide was removed by filtration, and the residue was purified by mplc (ethyl acetate/hexanes (1:4) to yield 1.5651 g (54%) of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06545023B2 |
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| Source dataset | uspto-grants-2003_04 |
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| ORD ID | ord-614990dbe74b4f5a94ab46b9806897b9 |
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| Source note | uspto-grants-2003_04 |
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