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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474083Generated: October 29, 2026

Triphenylphosphine → Triphenylphosphine Oxide

https://huagongshe.com/reaction/474083

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantMethanesulfonic acid 2-azido-1-(2-bromo-5-fluoro-pyridin-4-yl)-1-methyl-ethyl esterHCID 86668053—
SolventTetrahydrofuranHCID 8028—
ProductTriphenylphosphine OxideHCID 13097—
Product2-Bromo-5-fluoro-4-(2-methyl-aziridin-2-yl)-pyridineHCID 86668054—

Reaction Steps

A mixture of methanesulfonic acid 2-azido-1-(2-bromo-5-fluoro-pyridin-4-yl)-1-methyl-ethyl ester (2.1 g, 6.09 mmol) and PPh3 (1.597 g, 6.09 mmol) in THF (20 mL) was stirred at rt for 30 min. The reaction mixture was evaporated to dryness, the residue was taken up with TBME and 10% aq. citric acid soln. The aq. phase was reextracted with TBME, the combined org. phases were washed with H2O. The combined aq. phases were basified using 2N aq. NaOH soln. and three times extracted with TBME. The combined org. phases were dried over Na2SO4, filtered and concentrated to yield 2-bromo-5-fluoro-4-(2-methyl-aziridin-2-yl)-pyridine in a mixture with Ph3PO that was used for the next step without further purification, HPLC RtH4=0.96 min; ESIMS: 231, 233 [(M+H)+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637508B2
Source datasetuspto-grants-2014_01
ORD IDord-75249988c6b445a7bf5a2dfa73fd9524
Source noteuspto-grants-2014_01