Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 501280Generated: October 29, 2026

4-Methylmorpholine → trans-2-(4-Methyl-cyclohexylcarbamoyl)-cyclopropanecarboxylic acid methyl ester

https://huagongshe.com/reaction/501280

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantO-[(Ethoxycarbonyl)cyanomethylenamino]-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733286—
Reactantrac-(1R,2R)-2-(methoxycarbonyl)cyclopropane-1-carboxylic acidHCID 12510972—
ReactantHCID 178461305HCID 178461305—
SolventDimethylformamideHCID 6228—
Producttrans-2-(4-Methyl-cyclohexylcarbamoyl)-cyclopropanecarboxylic acid methyl esterHCID 6845681495.6%

Reaction Steps

Stir a solution of trans-cyclopropane-1,2-dicarboxylic acid monomethyl ester (Example 3a) (3.0 g, 20.8 mmol) and TOTU (8.5 g, 26 mmol) in DMF (300 mL) at ambient temperature for 20 min at which time add N-methylmorpholine (2.4 mL 22.9 mmol) and trans 4-methylcyclohexylamine 3.06 g, 27.0 mmol). After 3 h, remove the solvent and dissolve the residue in H2O/EtOAc. Extract the aqueous layer 3 more times with EtOAc and combine the extracts. Wash the extract with saturated NaHCO3 solution, brine and dry over MgSO4. Concentrate the solvent to afford the crude product, and purify by column chromatography over silica gel to give 4.76 g (95%) of colorless crystals, m/z=240 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772252B2
Source datasetuspto-grants-2010_08
ORD IDord-2b11d0b9d5d3465298f57f1b378e1252
Source noteuspto-grants-2010_08