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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1510367Generated: November 1, 2026

Methyl iodide → Ethyl 1-benzyloxycarbonyl-4-methoxy-3-methylpyrrolidine-3-carboxylate

https://huagongshe.com/reaction/1510367

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantEthyl 1-benzyloxycarbonyl-4-hydroxy-3-methylpyrrolidine-3-carboxylateHCID 68861273—
SolventDimethylformamideHCID 6228—
ProductEthyl 1-benzyloxycarbonyl-4-methoxy-3-methylpyrrolidine-3-carboxylateHCID 6886143966%

Reaction Steps

To a solution of ethyl 1-benzyloxycarbonyl-4-hydroxy-3-methylpyrrolidine-3-carboxylate (0.55 g, 1.8 mmol) in N,N-dimethylformamide (10 mL), methyl iodide (0.22 mL, 3.6 mmol) and sodium hydride (55% in oil, 117 mg, 2.7 mmol) were added in an ice bath, and the mixture was stirred at room temperature for 1 hour. Ice water was added to the reaction mixture, and the mixture was extracted with ethyl acetate (20 mL×3). The extract was washed with water (20 mL×3) and saturated aqueous solution of sodium chloride (20 mL) in this order, and dried with anhydrous sodium sulfate. After filtration, the filtrate was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (hexane:ethyl acetate, 2:1) to obtain 0.38 g (66%) of the title compound as a pale yellow oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08211910B2
Source datasetuspto-grants-2012_07
ORD IDord-9552a7ca61db440598ca838d4f1dc334
Source noteuspto-grants-2012_07