HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1019593Generated: October 30, 2026
Triphenylphosphine → HCID 86639063, compound
https://huagongshe.com/reaction/1019593
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | 3-Methoxybenzyl alcohol | HCID 81437 | — |
| Reactant | HCID 86639064 | HCID 86639064 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86639063 | HCID 86639063 | — |
Reaction Steps
0.089 mL (0.45 mmol) of diisopropyl azodicarboxylate is added dropwise under argon at 20° C., to a mixture of 260 mg (0.6 mmol) of supported triphenylphosphine (Argonaut PS-PPh3, loading 2.3 mmol/g), 57 mg (0.3 mmol) of 1H-pyrrolo[2,3-b]pyridine-2-ethyl carboxylate (WO07/010,138) and 62 mg (0.45 mmol) of 3-methoxybenzyl alcohol in 2.5 mL of tetrahydrofuran. The reactor is then sealed and the mixture is stirred for 3 days at 20° C. After this time, the reaction mixture is filtered, the solid residue is washed with 5 mL of tetrahydrofuran and the filtrate is concentrated at reduced pressure to give the expected product, which is used as it is in the rest of the synthesis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08716273B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-431af6da4dd845b1bc67ec49f2b9295f |
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| Source note | uspto-grants-2014_05 |
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