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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1032906Generated: October 30, 2026

Sodium Methoxide → HCID 178420905, compound

https://huagongshe.com/reaction/1032906

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium MethoxideHCID 10942334—
Reactant(Bromomethyl)cyclopentaneHCID 12723264—
ReactantHCID 178527894HCID 178527894—
SolventMethanolHCID 887—
ProductHCID 178420905HCID 17842090582.3%

Reaction Steps

Cyclopentylmethyl bromide (21 g; 0.13 mol) was added in one portion to 1,2,4-triazole-3-thiol (12.3 g; 0.12 mol) and sodium methoxide (7.1 g; 0.13 mol) in dry methanol (100 ml) under dry nitrogen. The mixture was stirred at room temperature for 3 days, refluxed for 3 h and evaporated. The residue was dissolved in ethyl acetate (200 ml) and water (100 ml), the organic phase separated, washed with water (100 ml), dried (Na2SO4), filtered and evaporated, to afford cyclopentylmethyl 1,2,4-triazol-3-yl sulfide (18.1 g; 82%) as a waxy, off-shite solid, m.p. 48°-55° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05308830
Source datasetuspto-grants-1994_05
ORD IDord-19766ef4ac3340eda100fabbae66fa29
Source noteuspto-grants-1994_05