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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 920639Generated: October 29, 2026

Benzyl Bromide → HCID 178420431, compound

https://huagongshe.com/reaction/920639

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantHCID 178507106HCID 178507106—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
ProductHCID 178420431HCID 17842043189.3%

Reaction Steps

Benzyl bromide (11.79 ml, 99 mmol) was added dropwise to a solution of sodium 1H-1,2,3-triazole-5-thiolate (12.2 g, 99 mmol) in ethanol (100 mL) at 0° C. The reaction mixture was allowed to warm to room temperature and stirred for 20 minutes. The reaction mixture was diluted with ethyl acetate (100 mL) and washed with water (100 mL), brine (100 mL) and dried (sodium sulphate). The solvent was removed to give 4-(benzylthio)-1H-1,2,3-triazole (16.9 g) as a white solid. LCMS (Method F, ES-API): RT 1.66 min, m+H=191.9; 1H NMR (400 MHz, CDCl3): δ 9.72 (1H, v br s), 7.47 (1H, s), 7.30-7.21 (5H, m), 4.12 (2H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273047B2
Source datasetuspto-grants-2016_03
ORD IDord-87fb0b7fdcb54b7d911ee8c497031cd4
Source noteuspto-grants-2016_03