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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2176884Generated: October 31, 2026

Methyl iodide → Ethyl 2-(pyridin-4-yl)propanoate

https://huagongshe.com/reaction/2176884

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantEthyl pyridine-4-acetateHCID 736321—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 2-(pyridin-4-yl)propanoateHCID 1165124050.7%

Reaction Conditions

Temperature-10 °C

Reaction Steps

A solution of ethyl 2-(pyridin-4-yl)acetate (1.00 g, 6.06 mmol) in THF (10 ml) was added dropwise to a suspension of sodium hydride (0.24 g, 6.06 mmol, 60%) in THF (10 ml) at −50° C. under an atmosphere of nitrogen. The reaction mixture was stirred for 1 h. Methyl iodide (2.10 ml, 33.6 mmol) in THF (10 ml) was added slowly at −50° C. over a period of 15 min, then the reaction mixture was warmed up to −10° C. and continued to stir for another 4 h. The reaction mixture was quenched with aqueous ammonium chloride and extracted with ethyl acetate (2×50 ml). The combined organic extracts were washed with brine (50 ml), dried over anhydrous sodium sulfate, filtered and concentrated under vacuo. The crude was washed with diethyl ether (10 ml) to get 550 mg (50.7%) of ethyl 2-(pyridin-4-yl)propanoate as a colorless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067888B2
Source datasetuspto-grants-2015_06
ORD IDord-b2a7646453604093a4b139ada6cd393a
Source noteuspto-grants-2015_06