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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 33492Generated: October 25, 2026

Water → 1-[2-(4-Allyloxy-benzylsulfanyl)-ethyl]-1H-[1,2,3]triazole

https://huagongshe.com/reaction/33492

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant[4-(Prop-2-en-1-yloxy)phenyl]methanethiolHCID 22242087—
Reactant2-(1H-1,2,3-triazol-1-yl)ethyl 4-methyl-1-benzenesulfonateHCID 22667111—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product1-[2-(4-Allyloxy-benzylsulfanyl)-ethyl]-1H-[1,2,3]triazoleHCID 2224207679%

Reaction Conditions

Temperature-30 °C

Reaction Steps

1.58 g (6.14 mmol) (4-allyloxy-phenyl)-methanethiol and 1.64 g (6.14 mmol) toluene-4-sulfonic acid 2-[1,2,3]triazol-1-yl-ethyl ester were dissolved in 15 ml N,N-dimethylformamide (DMF) and cooled to −30° C. 294 mg (12.3 mmol) 95% Sodium hydride were added, the mixture allowed to warm to room temperature (r.t.) and stirred for 12 h. 10 ml Water were added and the residue dissolved in dichloromethane. The organic phase was dried over Na2SO4, solvents removed and the remaining material purified by chromatography on silica gel (ethyl acetate/n-heptane 1:1) to yield 1.33 g (79%) yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07429605B2
Source datasetuspto-grants-2008_09
ORD IDord-6a37d3286e9249aabfc0d2ce2d01f0fc
Source noteuspto-grants-2008_09