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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1695327Generated: October 31, 2026

Triphenylphosphine → HCID 66643884, compound

https://huagongshe.com/reaction/1695327

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant(5-Methyl-3-phenyl-1,2-oxazol-4-yl)methanolHCID 2776149—
Reactant5-Hydroxy-1H-pyrazole-3-carboxylic acid methyl esterHCID 178498602—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66643884HCID 6664388427.9%

Reaction Steps

To a stirred solution of 5-hydroxy-2H-pyrazole-3-carboxylic acid methyl ester (1.30 g, 9.15 mmol) and (5-methyl-3-phenyl-isoxazol-4-yl)-methanol (1.73 g, 9.15 mmol) in THF (80 mL) at 5° C. under argon was added triphenylphosphine (3.12 g, 11.9 mmol), then diethyl azodicarboxylate (2.07 g, 11.9 mmol) was added dropwise. The reaction mixture was warmed to room temperature and stirred overnight. The reaction mixture was then evaporated. Purification by chromatography (silica, heptane:ethyl acetate=1:1 then dichloromethane:methanol=9:1) gave a colorless oil (800 mg) which was triturated with diisopropylether and further purified using a 5×50 cm Chiralpak AD column at room temperature using an isopropanol:heptane (2:8) mobile phase with UV detection at 220 nM to afford the title compound (250 mg, 9%) as a white solid. MS: m/e=328.3 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163728B2
Source datasetuspto-grants-2012_04
ORD IDord-27ba284d6b304aacbbd8eb4a79295903
Source noteuspto-grants-2012_04