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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389615Generated: October 31, 2026

benzyl 3-(4-cyclopropyl-4H-1,2,4-triazol-3-yl)phenylcarbamate → 3-(4-cyclopropyl-4H-1,2,4-triazol-3-yl)aniline

https://huagongshe.com/reaction/389615

Reaction equation

Participants

RoleNameHCIDCharge
Reactantbenzyl 3-(4-cyclopropyl-4H-1,2,4-triazol-3-yl)phenylcarbamateHCID 66851731—
SolventHydrogen BromideHCID 260—
Product3-(4-cyclopropyl-4H-1,2,4-triazol-3-yl)anilineHCID 5810304988.1%

Reaction Steps

[3-(4-Cyclopropyl-4H-[1,2,4]triazol-3-yl)-phenyl]-carbamic acid benzyl ester (60 mg, 0.17 mmol) was dissolved in HBr solution (1 mL, 33% in acetic acid) and the reaction mixture was stirred overnight. The solvent was removed and the residue was neutralized with saturated sodium bicarbonate solution before being poured into brine. The aqueous phase was extracted 5 times with ethyl acetate. The organic phase was dried with sodium sulfate and the solvent was removed to obtain 3-(4-cyclopropyl-4H-[1,2,4]triazol-3-yl)-phenylamine as an off-white powder (30 mg, 88%). 201.1 (M+1). 1H NMR of HBr salt (DMSO) d 9.24 (s, 1H), 7.50-7.63 (m, 3H), 6.6-8.0 (br, 4H+H2O), 3.65 ppm (m, 1H), 1.05 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08378108B2
Source datasetuspto-grants-2013_02
ORD IDord-c4cc3c8b73f74aea8ed5c62b0c8ec627
Source noteuspto-grants-2013_02