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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241677Generated: October 26, 2026

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

https://huagongshe.com/reaction/241677

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). R1=0.51 (3:2 cyclohexane:EtOAc).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653075B2
Source datasetuspto-grants-2014_02
ORD IDord-a0e59536df144b009924d9fc78337b73
Source noteuspto-grants-2014_02