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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 418611Generated: October 31, 2026

Cyclohexylamine → HCID 17805634, compound

https://huagongshe.com/reaction/418611

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexylamineHCID 7965—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl malonyl chlorideHCID 123460—
SolventDichloromethaneHCID 6344—
SolventOxolane--water (1/1)HCID 21881883—
ProductHCID 17805634HCID 1780563497%

Reaction Steps

To a solution of methyl 3-chloro-3-oxopropanoate (2.2 g, 16.1 mmol) in dry DCM (30 ml) at 0° C. was added cyclohexylamine (4.0 g, 40.3 mmol). The reaction mixture was stirred for 1 hr at room temperature. The reaction mixture was washed with diluted HCl, saturated NaHCO3 then brine well. The organic phase was collected, dried over anhydrous sodium sulfate then filtered and concentrated. The resultant crude amide was used directly in the next step with no additional purification (3.2 g, 100%). To a solution of this material (500 mg, 2.51 mmol) in THF/water (1:1, 20 ml) was added NaOH (200 mg, 5.02 mmol) and the mixture was stirred for 3 hrs at room temperature. The mixture was extracted with Et2O then the aqueous phase was acidified to pH 1 and extracted with EtOAc. The organic phase was collected, dried over anhydrous sodium sulfate then filtered and concentrated to afford the title compound 58 as a beige solid (450 mg, 97% yield). MS (m/z): 186.2 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093264B2
Source datasetuspto-grants-2012_01
ORD IDord-643450c6670648cdabb4c159fafc72b0
Source noteuspto-grants-2012_01