HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1032898Generated: October 30, 2026
Cyclohexane, (bromomethyl)- → HCID 178420906, compound
https://huagongshe.com/reaction/1032898
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cyclohexane, (bromomethyl)- | HCID 137636 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 178527894 | HCID 178527894 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178420906 | HCID 178420906 | 81.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05308830 |
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| Source dataset | uspto-grants-1994_05 |
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| ORD ID | ord-eafdb23d2bc64b2aad2b7459a3386ca1 |
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| Source note | uspto-grants-1994_05 |
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