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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1604114Generated: November 2, 2026

Triphenylphosphine → HCID 15867806, compound

https://huagongshe.com/reaction/1604114

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantTrifluoroiodomethaneHCID 16843—
ReactantMAGNESIUM SILICATE (synthetic)HCID 61680—
ReactantHCID 15867790HCID 15867790—
CatalystZincHCID 23994—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15867806HCID 1586780636%

Reaction Steps

Tris(dibenzylideneacetone)dipalladium(0) (11.4 mg, 0.0125 mmol), triphenylphosphine (13.1 mg, 0.05 mmol), zinc (powder) (36.8 mg, 56.3 mmol), and methyl (11R,12S,13E,15S,17R)-9-trifluoromethanesulfonyloxy-11,15-bis(tert-butyldimethylsiloxy)-17,20-dimethyl-7-thiaprosta-8,13-dienoate (218 mg, 0.282 mmol) in tetrahydrofuran (5 mL) were placed in an autoclave reactor, a small sized container of trifluoromethyl iodide was connected, and the inside of the reaction vessel was made the same pressure as the inside of the small sized container. The reaction vessel was made to vibrate in trifluoromethyl iodide atmosphere for 1 hour by an ultrasonic wave washer. Next, the unreacted trifluoromethyl iodide in the reaction vessel was removed to obtain the reaction solution which was passed through Florisil column. The solution thus obtained was concentrated under reduced pressure, then was purified by silica gel column chromotography (4to 10% ethyl acetate/hexane) to obtain methyl (11R,12S,13E,15S,17R)-9-trifluoromethyl-11,15-bis(tert-butyldimethylsiloxy)-17,20-dimethyl-7-thiaprosta-8,13-dienoate (72 mg, 36%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05990346
Source datasetuspto-grants-1999_11
ORD IDord-84487974cd6e4ec48337f5619ea94f81
Source noteuspto-grants-1999_11