Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1044424Generated: November 3, 2026

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

https://huagongshe.com/reaction/1044424

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 elctrospray 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 numberUS08563600B2
Source datasetuspto-grants-2013_10
ORD IDord-8c75c2064f9b4134941b23d27f09d276
Source noteuspto-grants-2013_10