Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725757Generated: November 1, 2026

Triphenylphosphine → HCID 86760815, compound

https://huagongshe.com/reaction/1725757

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantOzoneHCID 24823—
ReactantHCID 86760814HCID 86760814—
SolventDichloromethaneHCID 6344—
ProductHCID 86760815HCID 8676081583%

Reaction Steps

A solution of 3,5-bis(trifluoromethyl)benzyl 3-methylene-1-isopropylcyclopentane-carboxamide (910 mg, 2.31 mmol) in dichloromethane (50 mL) was cooled to −78° C. and a stream of ozone was passed through until the permanent blue color indicated complete consumption of the olefin. The excess ozone was purged with a stream of nitrogen, and triphenylphosphine (729 mg, 2.78 mmol) was added. The cooling bath was removed, and the reaction mixture was allowed to stir at ambient temperature overnight. The solvent was removed in vacuo, the residue was purified by column chromatography (silica gel, ethyl acetate:hexane/1:2) to give 760.7 mg (83%) of the desired product. 1H NMR (500 MHz, CDCl3): 7.81 (s, 1H), 7.74 (s, 2H), 6.16 (bs, 1H), 6.61 (m, 2H), 2.78 (bd, J=18.07 Hz, 1H), 2.40 to 2.20 (bm, 4H), 2.08-1.98 (m, 2H), 0.99 (d, J=6.86 Hz, 3H), 0.97 (d, J=6.87 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491737B2
Source datasetuspto-grants-2009_02
ORD IDord-06c587d4a6a242a69a7fb5c54d646fe3
Source noteuspto-grants-2009_02