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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant1,17-Diazido-3,6,9,12,15-pentaoxaheptadecaneHCID 18759534—
SolventHydrochloric AcidHCID 313—
SolventDiethyl EtherHCID 3283—
Product17-Azido-3,6,9,12,15-pentaoxaheptadecan-1-amineHCID 2189447695.7%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09180213B2
Source datasetuspto-grants-2015_11
ORD IDord-2c3e41aceae845b7ac6f1ec45b965654
Source noteuspto-grants-2015_11