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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1032898Generated: October 30, 2026

Cyclohexane, (bromomethyl)- → HCID 178420906, compound

https://huagongshe.com/reaction/1032898

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexane, (bromomethyl)-HCID 137636—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 178527894HCID 178527894—
SolventMethanolHCID 887—
ProductHCID 178420906HCID 17842090681.1%

Reaction Steps

Cyclohexylmethyl bromide (42 ml; 0.30 mol) was added over 5 min to 1,2,4-triazole-3-thiol (30.3 g; 0.30 mol) and sodium methoxide (17.3 g; 0.32 mol) in dry methanol (250 ml) under dry nitrogen. The mixture was refluxed for 4 h, stirred at room temperature overnight and evaporated. The residue was dissolved in ethyl acetate (400 ml) and water (200 ml). The organic phase is separated, washed with water (100 ml), dried (Na2SO4), filtered and its volume reduced by evaporation, causing a solid to precipitate. The solid was filtered off and dried, to afford cyclohexylmethyl 1,2,4-triazol-3-yl sulfide (48.0 g; 81%) as white plates, m.p. 74°-78° C. (Found, C: 54.98; H: 7.85; N: 21.32; S: 16.13. C9H15N3S requires C: 54.79; H: 7.66; N: 21.30; S: 16.25%). NMR - d(CDCl3 ; 90 MHz) 0.50-2.10 (11H, m), 3.1 (2H, d, J=6.4 Hz), 8.13 (1H, s) and 13.9 (1H, br s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05308830
Source datasetuspto-grants-1994_05
ORD IDord-eafdb23d2bc64b2aad2b7459a3386ca1
Source noteuspto-grants-1994_05