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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1026203Generated: November 2, 2026

Triphenylphosphine → tert-butyl {(1S)-2-[(6-bromopyridin-3-yl)oxy]-1-methylethyl}carbamate

https://huagongshe.com/reaction/1026203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Reactant2-Bromo-5-hydroxypyridineHCID 2762865—
Reactant1,1-Dimethylethyl N-((1S)-2-hydroxy-1-methylethyl)carbamateHCID 7023103—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Producttert-butyl {(1S)-2-[(6-bromopyridin-3-yl)oxy]-1-methylethyl}carbamateHCID 8666626157.4%

Reaction Steps

To a solution of 6-bromopyridin-3-ol (4.90 g), tert-butyl [(1S)-2-hydroxy-1-methylethyl]carbamate (4.93 g) and triphenylphosphine (11.06 g) in THF (100 mL) was added dropwise a toluene solution (1.9 M, 22 mL) of diisopropyl azodicarboxylate, and the mixture was stirred at room temperature for 3 hr. To the reaction mixture was added ethyl acetate, and the mixture was washed with water and saturated aqueous sodium hydrogen carbonate solution, dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (5.35 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729102B2
Source datasetuspto-grants-2014_05
ORD IDord-fb98801dd30d45f6a813feebea152a43
Source noteuspto-grants-2014_05