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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1638188Generated: November 2, 2026

Triphenylphosphine → (S)-3,5-di-(tert-butyldimethylsilyloxy)-pentan-2-one

https://huagongshe.com/reaction/1638188

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantOzoneHCID 24823—
Reactant(S)-1,3-Di-[(tert-butyldimethylsilyloxy)]-4-methyl-4-penteneHCID 11336893—
ReactantDiethylether pentaneHCID 21877078—
SolventOxygenHCID 977—
SolventDichloromethaneHCID 6344—
Product(S)-3,5-di-(tert-butyldimethylsilyloxy)-pentan-2-oneHCID 1178296770%

Reaction Steps

Ozone in O2 is directed at -78° C. through a solution of 1.610 g (4.67 mmol) of 11 in 200 ml of absolute dichloromethane (dry ice/acetone-cold bath). When starting compound 11 can no longer be detected by thin-layer chromatography in the solution, 3.89 g (14.83 mmol) of triphenylphosphine is added, and the cold bath is removed. The reaction batch is allowed to come slowly to room temperature, and the solvent is distilled off in a vacuum. Flash chromatography of the residue by a silica gel column with pentane/Et2O (50:1) yields 1.135 g (3.27 mmol, 70%) of 12.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06043372
Source datasetuspto-grants-2000_03
ORD IDord-96bf3ad6283c4d0ba544a40802859dbc
Source noteuspto-grants-2000_03