HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2284856Generated: October 31, 2026
Triphenylphosphine → HCID 118114178, compound
https://huagongshe.com/reaction/2284856
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | HCID 118114292 | HCID 118114292 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 118114178 | HCID 118114178 | 110.1% |
Reaction Steps
To a suspension of triphenylphosphine polymer supported (633 mg, 0.89 mmol) in THF (3 mL) was added a solution of methyl 5-((4-(azido(phenyl)methyl)phenoxy)-methyl)furan-2-carboxylate (293 mg, 0.81 mmol) in THF (6.1 mL) and H2O (0.12 mL). The reaction was stirred very slowly and heated at 60° C. for 18 h. Triphenylphosphine polymer supported (300 mg) and water (62 μL) were added and the heating was maintained at 60° C. for 5 h. The reaction was then allowed to cool to room temperature. The resin was removed by filtration, washed twice with THF and DCM. The combined organic phases were dried over MgSO4, filtered and the solvent removed in vacuo to give the title compound (301 mg) which was taken on to the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09145409B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-bab23cbe8d4e42caa5e75ca1bf5cceff |
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| Source note | uspto-grants-2015_09 |
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