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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 388261Generated: October 28, 2026

Methyl iodide → Ethyl 2-methoxy-2-(quinolin-5-yl)acetate

https://huagongshe.com/reaction/388261

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantEthyl 2-hydroxy-2-(quinolin-5-yl)acetateHCID 59185877—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 2-methoxy-2-(quinolin-5-yl)acetateHCID 5918593257%

Reaction Steps

To a solution of ethyl 2-hydroxy-2-(quinolin-5-yl)acetate (1.5 g, 6.5 mmol) in anhydrous THF in an oven-dried flask under argon was added iodomethane (1.2 mL, 19.2 mmol) and the mixture was cooled over an ice bath. NaH (60% in oil; 0.26 g, 6.5 mmol) was added and the mixture stirred for 1 hour over ice. After removing the ice bath, stirring was continued for an additional 3.25 hours, and more NaH (60%; 0.030 g, 0.75 mmol) was added. The mixture was stirred for 45 minutes then the reaction was quenched with brine and further diluted with water. The aqueous mixture was extracted with EtOAc and the combined organics were washed with water three times, brine once, dried over Na2SO4 and concentrated in vacuo. Purification by chromatography (50% EtOAc-hexanes) gave ethyl 2-methoxy-2-(quinolin-5-yl)acetate as a yellow oil (0.9 g, 57% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08377930B2
Source datasetuspto-grants-2013_02
ORD IDord-d263e518edd74002a1df0563705a682c
Source noteuspto-grants-2013_02