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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 259850Generated: October 25, 2026

Sodium Azide → 3-Azidomethyl-3-phenoxymethyloxetane

https://huagongshe.com/reaction/259850

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AzideHCID 33557—
Reactant[3-(Bromomethyl)oxetan-3-yl]methanolHCID 529264—
Reactant3-Chloromethyl-3-methyloxetane 3-chloromethyl-3-phenoxymethyloxetaneHCID 22404017—
Reactant[3-(Azidomethyl)oxetan-3-yl]methanolHCID 22404019—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Product3-Azidomethyl-3-phenoxymethyloxetaneHCID 2240402187%

Reaction Steps

As such, it has been discovered that monofunctional azidooxetane compounds, i.e., 3-azidomethyl-3-R1 -oxetanes, can also be prepared by combining a neat halooxetane with an aqueous metallic azide solution and a phase transfer catalyst (PTC). For example, using the process of the present invention, 3-chloromethyl-3-methyloxetane gives the corresponding 3-azidomethyl-3-methyloxetane (AMMO) in 97% yield. Moreover, 3-bromomethyl-3-hydroxymethyloxetane was previously converted to the corresponding 3-azidomethyl-3-hydroxymethyloxetane in acetone. Using the process of the present invention, however, 3-bromomethyl-3-hydroxymethyloxetane is converted to the corresponding 3-azidomethyl-3-hydroxymethyloxetane, without the use of an organic solvent, using an aqueous sodium azide solution and a phase transfer catalyst. The process of the present invention gives the same result with a faster rate of reaction and without the use of an organic solvent. In addition, 3-chloromethyl-3-methyloxetane 3-chloromethyl-3-phenoxymethyloxetane reacts with an aqueous solution of sodium azide in water with a PTC to give 3-azidomethyl-3-phenoxymethyloxetane in 87% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05523424
Source datasetuspto-grants-1996_06
ORD IDord-7f3adcefb4774a9fb881adc0618bb4e7
Source noteuspto-grants-1996_06