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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1257434Generated: October 31, 2026

Triphenylphosphine → HCID 66939147, compound

https://huagongshe.com/reaction/1257434

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantAmmonium ChlorideHCID 25517—
Reactantethyl 1H-pyrazole-4-carboxylateHCID 142179—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantHCID 7245333HCID 7245333—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66939147HCID 6693914759.3%

Reaction Steps

A solution of the compound (0.40 g) obtained in Example 127b, ethyl 1H-pyrazole-4-carboxylate (0.26 g) and triphenylphosphine (0.49 g) in tetrahydrofuran (8 mL) was cooled in an ice bath, diethyl azodicarboxylate (0.30 mL) was added, and the mixture was stirred at the same temperature for 1 hr. Saturated aqueous ammonium chloride solution was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The obtained organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by column chromatography (carrier: silica gel, eluent: hexane/ethyl acetate) to give the title compound (0.35 g) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461348B2
Source datasetuspto-grants-2013_06
ORD IDord-77a16f7d30484b5aa0759f5c21e2b7d2
Source noteuspto-grants-2013_06