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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 280637Generated: October 30, 2026

Sodium Azide → 3-(4-Chlorobenzoyl)-benzyl azide

https://huagongshe.com/reaction/280637

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AzideHCID 33557—
Reactant3-(4-Chlorobenzoyl)benzyl bromideHCID 13649653—
SolventEthanolHCID 702—
Product3-(4-Chlorobenzoyl)-benzyl azideHCID 13649660100.1%

Reaction Steps

A mixture of 3-(4-chlorobenzoyl)benzyl bromide (4.2 g, 13.6 mmol) and sodium azide (1.32 g, 20.3 mmol) in ethanol (40 ml) was refluxed for 5 hours, cooled to ambient temperature, and kept 16 hours. The mixture was filtered and the solids were washed twice with ethanol. The combined filtrate and washes were evaporated to dryness under vacuum and the residue was treated with diethyl ether and filtered. The filtrate was evaporated to dryness under vacuum and dried to provide 3.7 g (100%) of 3-(4-chlorobenzoyl)-benzyl azide, m.p. 43°-45° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04590201
Source datasetuspto-grants-1986_05
ORD IDord-797ab928d8754b319797ffa3ce390464
Source noteuspto-grants-1986_05