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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1927126Generated: November 2, 2026

Triphenylphosphine → 2-{[(2-Bromoethyl)oxy]methyl}naphthalene

https://huagongshe.com/reaction/1927126

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantN-bromobutanimideHCID 67184—
Reactant2-[(2-Naphthalenylmethyl)oxy]ethanolHCID 59000353—
SolventDichloromethaneHCID 6344—
SolventAluminumHCID 5359268—
Product2-{[(2-Bromoethyl)oxy]methyl}naphthaleneHCID 6896063943.1%

Reaction Steps

A solution of N-bromosuccinimide (272 mg, 1.53 mmol) in DCM (2.5 mL) was added to resin-bound triphenylphosphine (510 mg, 1.53 mEquiv, Fluka) in DCM (2.5 mL), and the reaction was stirred at rt for 10 min. A solution 2-[(2-naphthalenylmethyl)oxy]ethanol (101 mg, 0.499 mmol) in DCM (1.5 mL) was added to the reaction, and the residual alcohol was transferred with additional DCM (1.5 mL). The reaction vial was capped, wrapped in aluminum foil, and stirred at rt for 20 h. The reaction was filtered through a SPE cartridge (5 g silica) eluting with the following 10 mL fractions: DCM (fraction 1), 30% EtOAc/hexanes (fraction 2), and 50% EtOAc/hexanes (fraction 3) to give the title compound (57 mg, 43%). The product was characterized by 1H NMR (400 MHz) in CDCl3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08183257B2
Source datasetuspto-grants-2012_05
ORD IDord-80df5bba0cf34c2994c0f7f709646f1b
Source noteuspto-grants-2012_05