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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2167618Generated: October 31, 2026

Triphenylphosphine → HCID 67027645, compound

https://huagongshe.com/reaction/2167618

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 28414031HCID 28414031—
SolventDichloromethaneHCID 6344—
SolventAluminumHCID 5359268—
ProductHCID 67027645HCID 6702764547%

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 of 4-{[(2-hydroxyethyl)oxy]methyl}benzonitrile (95 mg, 0.536 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 (60 mg, 47%). The product was characterized by 1H NMR (400 MHz) in CDCl3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045469B2
Source datasetuspto-grants-2015_06
ORD IDord-c7c2003f56a14dc3a8599d6a8df946cc
Source noteuspto-grants-2015_06