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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1983031Generated: November 2, 2026

Thionyl Chloride → 1-(chloromethyl)-3-t-butyl-1H-1,2,4-triazole hydrochloride

https://huagongshe.com/reaction/1983031

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant3-t-butyl-1H-1,2,4-triazole1-ylmethanolHCID 57712418—
Product1-(chloromethyl)-3-t-butyl-1H-1,2,4-triazole hydrochlorideHCID 23149120—

Reaction Steps

The mixture of 1.38 g of 3-t-butyl-1H-1,2,4-triazole1-ylmethanol and 2.7 ml of thionyl chloride was stirred under reflux condition for 3 hours. After the reaction mixture was cooled to room temperature, the reaction mixture was concentrated under reduced pressure. The residue was recrystallized from hexane to obtain 1.72 g of 3-t-butyl-1-(chloromethyl)-1H-1,2,4-triazole hydrochloride. 1H-NMR (CDCl3, TMS, δ (ppm)): 1.36 (9H, s), 5.83 (2H, s), 8.17 (1H, s)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07541374B2
Source datasetuspto-grants-2009_06
ORD IDord-0233433b0e7c40e2b7795291e72393a0
Source noteuspto-grants-2009_06