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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2358163Generated: November 3, 2026

Triphenylphosphine → HCID 67544981, compound

https://huagongshe.com/reaction/2358163

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant3-Fluorobenzylic alcoholHCID 68008—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantEthyl 5-phenyl-1H-pyrrolo[2,3-c]pyridine-2-carboxylateHCID 67544750—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67544981HCID 6754498178.1%

Reaction Conditions

Temperature20 °C

Reaction Steps

0.72 g (5.63 mmol) of 3-fluorobenzyl alcohol, 1.47 g (5.63 mmol) of triphenylphosphine and then 1.01 g (5.63 mmol) of diethyl azodicarboxylate are successively added to a solution, stirred at 0° C. under argon, of 1 g (3.76 mmol) of ethyl 5-phenyl-1H-pyrrolo[2,3-c]pyridine-2-carboxylate, obtained in step 18.3, in 30 ml of dry tetrahydrofuran. The mixture is then stirred for 20 hours at 20° C., concentrated under reduced pressure and then purified by chromatography on a column of silica (eluents: heptane/ethyl acetate). 1.1 g of the expected product are thus isolated in the form of a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07763636B2
Source datasetuspto-grants-2010_07
ORD IDord-a9ed84bfcc70440ba85d047537a15f4d
Source noteuspto-grants-2010_07