HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 728463Generated: October 30, 2026
Triphenylphosphine → HCID 14835005, compound
https://huagongshe.com/reaction/728463
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Hydrazoic acid | HCID 24530 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | HCID 14834986 | HCID 14834986 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 14835005 | HCID 14835005 | 81% |
Reaction Steps
To a stirred solution of 1.02 g (2.25 mM) of 2-(5-methyl-1H-tetrazol-1-yl)-3-octadecylcarbamoyloxypropanol Vi2, 885 mg (3.38 mM) of triphenylphosphine, and 1.9 ml (3.38 mM) of 1.8 mM benzene solution of hydrazoic acid in 50 ml of tetrahydrofurane at -50° C. is added 0.53 ml (3.38 mM) of diethyl azodicarboxylate dropwise and the mixture is raised to room temperature during 2 hr. Subsequently, 150 mg of 10% palladium carbon is added to the mixture which is stirred under hydrogen gas for 30 minutes. After 10% palldium carbon filtered off, the solvent is evaporated. The residue obtained is purified by column silica gel chromatography using ethyl acetate-choroform/methanol (9/1) mixture as an eluent and 0.82 g (81% yield) of the title compound is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05047540 |
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| Source dataset | uspto-grants-1991_09 |
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| ORD ID | ord-6a06a12b8ce84f879a2d4c38469e06c2 |
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| Source note | uspto-grants-1991_09 |
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