Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 407944Generated: October 26, 2026

Triphenylphosphine → HCID 86688098, compound

https://huagongshe.com/reaction/407944

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant2-Bromo-5-hydroxypyridineHCID 2762865—
Reactant2-Hydroxy-gamma-butyrolactone, (2R)-HCID 7157070—
SolventTolueneHCID 1140—
ProductHCID 86688098HCID 8668809879.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of (R)-3-hydroxydihydrofuran-2(3H)-one (500 mg, 4.9 mmol) in toluene (15 mL) was added triphenylphosphine (1.54 g, 5.88 mmol) and 6-bromopyridin-3-ol (1.02 g, 5.88 mmol). The solution was cooled to 0° C. and degassed with nitrogen bubble for 10 minutes. Di-tert-butyl diazene-1,2-dicarboxylate was dissolved in toluene (5 mL) and added over a 5 minute period. The reaction was allowed to stir for 12 hours with warming to ambient temperature. The reaction was concentrated in vacuo and the resulting material purified by silica gel chromatography eluting 1:1 hexanes/EtOAc to yield (S)-3-(6-bromopyridin-3-yloxy)dihydrofuran-2(3H)-one (1.0 g, 79%) as an off white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754226B2
Source datasetuspto-grants-2014_06
ORD IDord-cf7dbac727cd4c9f8ea45bcd593f7c7f
Source noteuspto-grants-2014_06