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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241678Generated: October 31, 2026

3-bromo-5-nitrophenyl-1-methyl-1H-tetrazole → 3-Bromo-5-(1-methyl-1H-tetrazol-5-yl)-phenylamine

https://huagongshe.com/reaction/241678

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-bromo-5-nitrophenyl-1-methyl-1H-tetrazoleHCID 22252690—
CatalystNickelHCID 935—
SolventEthyl AcetateHCID 8857—
Product3-Bromo-5-(1-methyl-1H-tetrazol-5-yl)-phenylamineHCID 6673330415.4%

Reaction Steps

A solution of 5-(3-Bromo-5-nitro-phenyl)-1-methyl-1H-tetrazole (2.1 g) in EtOAc (100 ml) was hydrogenated on a H-cube® apparatus at 20° C., room pressure with a flow rate of 1 ml/min using a Raney-Ni cartridge. After reaction completion, the mixture was concentrated in vacuum and triturated with MeOH. The solid was filtered and further triturated and air-dried to give the title compound (290 mg). Rt 1.25 min (method D).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653075B2
Source datasetuspto-grants-2014_02
ORD IDord-1eb42581ce744241b77c3d5c6ed19397
Source noteuspto-grants-2014_02