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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1962948Generated: November 1, 2026

Triphenylphosphine → 5-(5-Methyl-3-phenyl-isoxazol-4-ylmethoxy)-pyridine-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1962948

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant(5-Methyl-3-phenyl-1,2-oxazol-4-yl)methanolHCID 2776149—
Reactant5-Hydroxypyridine-2-carboxylic acid ethyl esterHCID 23145820—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
Product5-(5-Methyl-3-phenyl-isoxazol-4-ylmethoxy)-pyridine-2-carboxylic acid ethyl esterHCID 6664439543.2%

Reaction Steps

To a stirred solution of (5-methyl-3-phenyl-4-isoxazolyl)methanol (570 mg, 3.01 mmol) and 5-hydroxy-pyridine-2-carboxylic acid ethyl ester (655 mg, 3.92 mmol) in THF (15 mL) under argon was added triphenylphosphine (1.03 g, 3.93 mmol). Diethyl azodicarboxylate (1.71 mL of a 40% solution in toluene, 682 mg, 3.92 mmol) was added dropwise. After 20 h the reaction mixture was concentrated in vacuo, water was added, and the reaction mixture extracted with ethyl acetate. The combined organic extracts were dried, filtered and concentrated then purified by chromatography (silica, 10 to 60% ethyl actetate in heptane) afforded the title compound (440 mg, 43%) as a pink oil. MS: m/e=339.3 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415379B2
Source datasetuspto-grants-2013_04
ORD IDord-96259b67cf9a4471998d875621af99fa
Source noteuspto-grants-2013_04