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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1647133Generated: October 31, 2026

Cyclohexylamine → HCID 10760075, compound

https://huagongshe.com/reaction/1647133

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexylamineHCID 7965—
ReactantHCID 57259964HCID 57259964—
SolventTetrahydrofuranHCID 8028—
ProductHCID 10760075HCID 1076007565.9%

Reaction Steps

To a solution of benzyl (2S)-2-chlorocarbonyloxy-4-methylvalerate (0.56 g) in tetrahydrofuran (11 ml) was added cyclohexylamine (0.40 g) at room temperature. After being stirred for 10 minutes, the solvent was removed by evaporation under reduced pressure, and the residue was dissolved in ethyl acetate (30 ml). The solution was washed with 1N HCl, water and brine successively. The organic layer was dried over magnesium sulfate and concentrated in vacuo. The residual solid was triturated with hexane to give benzyl (2S)-2-cyclohexylcarbamoyloxy-4-methylvalerate (0.45 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05430022
Source datasetuspto-grants-1995_07
ORD IDord-78a357f5159545818bf6944e4d08a7af
Source noteuspto-grants-1995_07