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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1737448Generated: October 31, 2026

Triphenylphosphine → HCID 21842622, compound

https://huagongshe.com/reaction/1737448

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantBromineHCID 24408—
ReactantN-(2-(3-Chlorophenyl)-5-hydroxypentyl)-N-methylbenzenesulfonamideHCID 21842614—
SolventAcetonitrileHCID 6342—
ProductHCID 21842622HCID 21842622—

Reaction Steps

Bromine was added to a solution of triphenylphosphine (41.4 mg, 0.158 mmol) in 0.50 mL of acetonitrile until the red color persisted, and a small additional quantity of triphenylphorsphine was then added to consume the excess bromine. A solution of N-(2-(3-chlorophenyl)-5-hydroxypentyl)-N-methylbenzenesulfonamide (38.7 mg, 0.105 mmol) in 0.3 mL of acetonitrile was added. After stirring for 1 h, the reaction was quenched by a solution of sodium sulfite (20 mg) dissolved in 1.0 mL of water. The mixture was diluted with 15 mL of sodium bicarbonate and extracted with 2×20 mL of ethyl acetate. The organic layers were washed with 15 mL of brine, dried over sodium sulfate and concentrated. The crude product was purified by flash column chromatography on silica gel, eluting with of 10% ethyl acetate in hexane to give 23 mg the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05962462
Source datasetuspto-grants-1999_10
ORD IDord-240198b4a6924a729796830aac143154
Source noteuspto-grants-1999_10