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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620628Generated: October 31, 2026

(1R,2R)-2-Aminocyclohexanol → HCID 178518169, compound

https://huagongshe.com/reaction/1620628

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(1R,2R)-2-AminocyclohexanolHCID 735777—
Reactant4-Sulfanylidene-1,3-thiazolidin-2-oneHCID 1539595—
SolventEthanolHCID 702—
ProductHCID 178518169HCID 17851816929.8%

Reaction Steps

To a solution of trans-2-aminocyclohexanol (1.00 g) in ethanol (50 mL) was added 4-thioxo-1,3-thiazolidin-2-one (1.19 g), and the mixture was heated under reflux overnight. The reaction mixture was cooled to room temperature, the precipitate was removed, and the solvent of the filtrate was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (NH, tetrahydrofuran). The obtained powder was washed with ethyl acetate to give the title compound (554 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772277B2
Source datasetuspto-grants-2014_07
ORD IDord-0a3bc08c5e03449e935c550194de1060
Source noteuspto-grants-2014_07