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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1749664Generated: November 1, 2026

Hydrochloric Acid → HCID 178451823, compound

https://huagongshe.com/reaction/1749664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantBenzyltrimethylammoniumtribromideHCID 53442637—
ReactantHCID 178451807HCID 178451807—
SolventDichloromethaneHCID 6344—
ProductHCID 178451823HCID 17845182387%

Reaction Steps

To a stirred solution of tert-butyl 4-(1H-1,2,4-triazol-3-yl)piperidine-1-carboxylate (22 g, 87.19 mmol) in dichloromethane (250 mL) was added sodium hydroxide 2N (131 mL, 261.58 mmol). The reaction mixture was vigorously stirred with mechanical stirring and a solution of benzyltrimethylammonium tribromide (37.4 g, 95.91 mmol) in dichloromethane (250 mL) was then added dropwise, keeping temperature around 15° C. The reaction mixture was left to stir at room temperature for 1 h and 2N HCl was added to give a pH of 5 (keeping temperature around 15° C.). The phases were decanted and the organic phase was washed with H2O (2×1 L), dried over MgSO4, filtered and concentrated to afford tert-butyl 4-(5-bromo-1H-1,2,4-triazol-3-yl)piperidine-1-carboxylate (25.00 g, 87%) as an off-white solid: 1H NMR Spectrum; (CDCl3) 1.46 (9H, s), 1.67-1.84 (2H, m), 1.90-2.13 (2H, m), 2.77-2.96 (2H, m), 2.98-3.10 (1H, m), 3.94-4.35 (2H, m); Mass Spectrum [M+H]+=no mass ion.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156831B2
Source datasetuspto-grants-2015_10
ORD IDord-5517e7018ef04ac7bafd2d1d3e9bfdd6
Source noteuspto-grants-2015_10