HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1870286Generated: October 31, 2026
Triphenylphosphine → HCID 15453937, compound
https://huagongshe.com/reaction/1870286
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | tert-butyl N-(2-hydroxyethyl)carbamate | HCID 2733206 | — |
| Reactant | HCID 178518983 | HCID 178518983 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 15453937 | HCID 15453937 | 68.9% |
Reaction Steps
To a solution of triphenylphosphine (0.95 g) in tetrahydrofuran (20 ml) was added diethyl azodicarboxylate (0.63 g) with stirring at 5° C., then stirred at the same temperature for 15 minutes. To a reaction mixture, 3-hydroxy-1,2-benzisoxazole (0.45 g) was added and stirred for 15 minutes, then N-t-butoxycarbonyl ethanolamine (0.53 g) was added and the mixture stirred at room temperature for 24 hour. The solvent was evaporated under reduced pressure and residue was purified by silica gel column chromatography with cyclohexane/ethyl acetate (9/1) as an eluent, to give the title compound (0.63 g, 68%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06096771 |
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| Source dataset | uspto-grants-2000_08 |
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| ORD ID | ord-53c22f31bb034765bccf25548bcaa88b |
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| Source note | uspto-grants-2000_08 |
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