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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2104282Generated: October 30, 2026

Ethyl 2-hydroxyisobutyrate → 2-Ethoxy-5-(methanesulfonyl)pyridine

https://huagongshe.com/reaction/2104282

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-hydroxyisobutyrateHCID 6653—
ReactantSodium hydrideHCID 24758—
Reactant2,5-Bis(methylsulfonyl)pyridineHCID 13102675—
SolventDimethylformamideHCID 6228—
Product2-Ethoxy-5-(methanesulfonyl)pyridineHCID 22270327—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of ethyl 2-hydroxyisobutyrate (0.41 mL, 3.0 mmol), 2,5-bis(methyl sulfonyl) pyridine (J. Heterocycl. Chem. 1985, 22, 1583) (0.70 g, 3.0 mmol) and sodium hydride (60% dispersion in mineral oil, 0.14 g, 3.6 mmol) in 30 mL of anhydrous DMF was heated at 80° C. overnight. The reaction mixture was cooled to room temperature, and was partitioned between saturated aqueous ammonium chloride (200 mL) and ether (200 mL). The organic layer was separated and was washed with water and brine, dried over anhydrous sodium sulfate, filtered and concentrated to dryness, and the residue was purified by flash column chromatography on silica gel eluting with 0 to 80% ethyl acetate in hexane to give the title compound as a 1:1 mixture with 2-ethoxy-5-methylsulfonylpyridine. LC-MS: m/e 288 (M+H)+ (0.70 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576239B2
Source datasetuspto-grants-2009_08
ORD IDord-f83f53eb129b43ef96270e60ead74498
Source noteuspto-grants-2009_08