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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 884319Generated: November 1, 2026

Triphenylphosphine → 17-Azido-3,6,9,12,15-pentaoxaheptadecan-1-amine

https://huagongshe.com/reaction/884319

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 of 22 g (95%) of a yellow oil. The product was identified by electrospray mass spectrometry (ESI-MS) (MH+ calculated: 307.19; found 307.4). The crude oil was used in the nest step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08241606B2
Source datasetuspto-grants-2012_08
ORD IDord-7cf6703238134436a994ef962ca88675
Source noteuspto-grants-2012_08