HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2358163Generated: November 3, 2026
Triphenylphosphine → HCID 67544981, compound
https://huagongshe.com/reaction/2358163
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 3-Fluorobenzylic alcohol | HCID 68008 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | Ethyl 5-phenyl-1H-pyrrolo[2,3-c]pyridine-2-carboxylate | HCID 67544750 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67544981 | HCID 67544981 | 78.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07763636B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-a9ed84bfcc70440ba85d047537a15f4d |
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| Source note | uspto-grants-2010_07 |
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