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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2387396Generated: October 25, 2026

Methyl iodide → Methyl 2-((tert-butoxycarbonyl)amino)-3-cyclohexylpropanoate

https://huagongshe.com/reaction/2387396

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
ReactantBoc-DL-Cha-OHHCID 2817530—
SolventDimethylformamideHCID 6228—
ProductMethyl 2-((tert-butoxycarbonyl)amino)-3-cyclohexylpropanoateHCID 426460297.9%

Reaction Steps

To a solution of 2-tert-butoxycarbonylamino-3-cyclohexyl-propionic acid (3.0 g, 11.1 mmol) and potassium carbonate (1.5 g, 11.1 mmol) in N,N-dimethylformamide (20 mL) was added methyl iodide (0.795 μL; 12.1 mmol). The reaction mixture was stirred at room temperature overnight. To the reaction mixture was added ethyl acetate (100 mL) and the solution was washed with water (3×100 mL). The organic layer was dried over anhydrous sodium sulfate, filtered, and concentrated to give the title intermediate as an oil (3.1 g) which was used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268863B2
Source datasetuspto-grants-2012_09
ORD IDord-2de1330834d74e1ea6f8b23f4a924318
Source noteuspto-grants-2012_09