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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36178Generated: October 26, 2026

Lithium azide → 4-Azidomethyl-2'-cyanobiphenyl

https://huagongshe.com/reaction/36178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium azideHCID 88163—
Reactant4'-(Bromomethyl)-2-cyanobiphenylHCID 1501912—
SolventDimethyl SulfoxideHCID 679—
Product4-Azidomethyl-2'-cyanobiphenylHCID 1035398961%

Reaction Steps

A mixture of 1.97 g (725 mole) of 4-bromomethyl-2'-cyanobiphenyl (EP 253,310), 445 mg (9.1 mmole) of lithium azide and 5 ml of dry DMSO was stirred at room temperature under nitrogen for one hour and then partitioned between 100 ml of ether and 100 ml of H2O. The organic phase was washed with 3×100 ml of H2O, then dried (MgSO4), filtered, and concentrated in vacuo to give a residual oil which solidified on standing. This solid was triturated with petroleum ether, collected on a filter, washed with petroleum ether and dried overnight to yield 1.15 g (61%) of the title compound as white crystals, mp 69°-70° C.; mass spectrum (EI) m/e 234 (M+). TLC in 4:1 hexane-EtOAc showed only minor impurities and the material was of sufficient purity to use in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05411980
Source datasetuspto-grants-1995_05
ORD IDord-8aaecded671844a2a92627ce27ea0413
Source noteuspto-grants-1995_05