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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716288Generated: November 1, 2026

Triphenylphosphine → 3-(4'-Bromo-biphenyl-4-yloxymethyl)-2-methoxy-pyridine

https://huagongshe.com/reaction/1716288

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant4-Bromo-4'-hydroxybiphenylHCID 95093—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
Reactant(2-Methoxypyridin-3-yl)methanolHCID 10630565—
SolventTetrahydrofuranHCID 8028—
Product3-(4'-Bromo-biphenyl-4-yloxymethyl)-2-methoxy-pyridineHCID 68512724—

Reaction Steps

To a mixture of PPh3 (0.53 g, 2.03 mmol) and DIAD (0.4 mL, 2.03 mmol) in dry THF (3 mL) at 0° C. was added a mixture of (2-methoxy-pyridin-3-yl)-methanol (0.18 g, 1.27 mmol) from Step A and 4′-bromo-biphenyl-4-ol (0.33 g, 1.33 mmol) in dry THF (2 mL). After 1 hr, the reaction was warmed to room temperature and monitored by TLC. After the reaction was completed (˜4 h), the reaction mixture was concentrated under vacuo and then diluted with EtOAc. The precipitates were filtered. The filtrate was brought to the usual work-up. The resulting crude product was purified by chromatography (silica gel, 15% EtOAc/hexanes) to give the titled compound. MS: 370, 372 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803793B2
Source datasetuspto-grants-2010_09
ORD IDord-d9b6a02ac3aa427588daf5874ea11e16
Source noteuspto-grants-2010_09