HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 709335Generated: October 29, 2026
Triphenylphosphine → 17-Azido-3,6,9,12,15-pentaoxaheptadecan-1-amine
https://huagongshe.com/reaction/709335
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 1,17-Diazido-3,6,9,12,15-pentaoxaheptadecane | HCID 18759534 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 17-Azido-3,6,9,12,15-pentaoxaheptadecan-1-amine | HCID 21894476 | 95.7% |
Reaction Steps
To a vigorously stirred suspension of 1,17-diazido-3,6,9,12,15-pentaoxaheptadecane (25 g, 75 mmol) in 5% HCl (200 mL) was added a solution of triphenylphosphine (19.2 g, 73 mmol) in ether (150 mL) over 3 hrs at room temperature. The reaction mixture was stirred for additional 24 hrs. The phases were separated and the aqueous phase was extracted with dichloromethane (3×40 mL). The aqueous phase was cooled in an ice/water bath and the pH was adjusted to 12 by addition of solid potassium hydroxide. The aqueous phase was concentrated and the product was taken up in dichloromethane (150 mL). The organic phase was dried (Na2SO4) and concentrated giving a yellow oil 22 g (95%). The product was identified by electrospray mass spectrometry (ESI-MS) (MH+ calculated: 307.19. found 307.4). The crude oil was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09180213B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-2c3e41aceae845b7ac6f1ec45b965654 |
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| Source note | uspto-grants-2015_11 |
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