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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1093464Generated: October 25, 2026

Triphenylphosphine → 1-(3-Bromopropyl)naphthalene

https://huagongshe.com/reaction/1093464

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantN-bromobutanimideHCID 67184—
Reactant3-(Naphthalen-1-yl)propan-1-olHCID 14711518—
SolventDichloromethaneHCID 6344—
Product1-(3-Bromopropyl)naphthaleneHCID 1471151990.2%

Reaction Steps

Compound 73-1 (4.70 g) was dissolved in methylene chloride (50 ml), triphenylphosphine (7.13 g) and N-bromosuccinimide (4.84 g) were added under ice-cooling, and the mixture was stirred under ice-cooling for 2 hr, and further at room temperature for 15 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 (100 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 (5.67 g) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129361B2
Source datasetuspto-grants-2012_03
ORD IDord-762941dcbcd7428ea34b89cca6e9862b
Source noteuspto-grants-2012_03