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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 499671Generated: October 29, 2026

Triphenylphosphine → HCID 24694511, compound

https://huagongshe.com/reaction/499671

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 68461234HCID 68461234—
SolventDichloromethaneHCID 6344—
SolventAluminumHCID 5359268—
ProductHCID 24694511HCID 24694511104.3%

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 2-({[3-(methyloxy)phenyl]methyl}oxy)ethanol (114 mg, 0.626 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 (160 mg, title compound and impurity). The product was characterized by 1H NMR (400 MHz) in CDCl3. The purity of the compound was good enough to carry on the next reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07767691B2
Source datasetuspto-grants-2010_08
ORD IDord-4f58443fee564a51a30adabf9f236dc3
Source noteuspto-grants-2010_08