HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 573518Generated: October 31, 2026
Triphenylphosphine → HCID 86699450, compound
https://huagongshe.com/reaction/573518
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Di-tert-butyl azodicarboxylate | HCID 97268 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | HCID 86699451 | HCID 86699451 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86699450 | HCID 86699450 | — |
Reaction Steps
Triphenyl phosphine (14.4 g, 55 mmol) was dissolved in THF and cooled to 0° C. under nitrogen. Di-tertbutyl azodicarboxylate (13.7 g, 59.5 mmol) was added slowly and the reaction was stirred for 30 mins. Then the alcohol (20 g, 45.8 mmol) was added dropwise and allowed to stir for 10 mins, then diphenyl phosphorylazide (15.1 g, 55 mmol) was added and allowed to stir overnight, warming to ambient temperature. The reaction was evaporated to dryness in vacuo and directly loaded onto a silica gel column and eluted with 0-10% ethyl acetate/hexane gradient to provide (2S)-2-azidoundecyl(9Z,12Z)-octadeca-9,12-dien-1-yl ether which was carried directly into the next reaction without characterization.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09029604B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-499c31acb1984c408acbe4e6f4e0bedd |
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| Source note | uspto-grants-2015_05 |
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