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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2059641Generated: October 30, 2026

Sodium Azide → 3-bromo-5-nitrophenyl-1-methyl-1H-tetrazole

https://huagongshe.com/reaction/2059641

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AzideHCID 33557—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantSodium BicarbonateHCID 516892—
Reactant3-Bromo-N-methyl-5-nitrobenzamideHCID 22252686—
SolventDichloromethaneHCID 6344—
Product3-bromo-5-nitrophenyl-1-methyl-1H-tetrazoleHCID 2225269044.1%

Reaction Steps

To a solution of 3-bromo-N-methyl-5-nitro-benzamide (0.6 g) in DCM (15 ml) at −15° C. was added triflic anhydride (0.6 ml) and the reaction stirred for 30 min. Sodium azide (226 mg) was added and the reaction allowed to warm to room temperature and stirred further overnight. NaHCO3(aq) was added to neutralise the reaction and the mixture extracted into EtOAc. The organic layer was separated, dried and concentrated in vacuum and the residue purified by flash chromatography (9:1 to 2:8 cyclohexane:EtOAc) to give the title compound (290 mg). Rf=0.51 (3:2 cyclohexane:EtOAc).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08278302B2
Source datasetuspto-grants-2012_10
ORD IDord-e3a0e16ac7f0462b81d2a8375ae3865c
Source noteuspto-grants-2012_10