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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1093498Generated: November 1, 2026

Triphenylphosphine → 1-(3-Bromopropyl)-3-nitrobenzene

https://huagongshe.com/reaction/1093498

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantN-bromobutanimideHCID 67184—
Reactant3-(3-Nitrophenyl)propan-1-olHCID 11332842—
SolventDichloromethaneHCID 6344—
Product1-(3-Bromopropyl)-3-nitrobenzeneHCID 1484218994.5%

Reaction Steps

Compound 95-1 (220 mg) was dissolved in methylene chloride (10 ml), triphenylphosphine (350 mg) and N-bromosuccinimide (238 mg) were added under ice-cooling, and the mixture was stirred under ice-cooling for 1 hr, and at room temperature for 12 hr. The reaction mixture was washed with water and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. Diethyl ether (30 ml) was added, and the precipitated triphenylphosphine oxide was filtered off. The concentrate of the filtrate was purified by silica gel column chromatography to give the object product (280 mg) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129361B2
Source datasetuspto-grants-2012_03
ORD IDord-ded5adde28404bee858bebb3700066fa
Source noteuspto-grants-2012_03