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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 714449Generated: October 25, 2026

Tetrahydrofuran → rac-4-(1-Hydroxyethyl)-N-methylpyridine-2-carboxamide

https://huagongshe.com/reaction/714449

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium BicarbonateHCID 516892—
Reactant4-formyl-N-methylpicolinamideHCID 21963889—
ReactantHCID 178418573HCID 178418573—
SolventEthyl AcetateHCID 8857—
Productrac-4-(1-Hydroxyethyl)-N-methylpyridine-2-carboxamideHCID 68047396—

Reaction Steps

At 0° C. and under argon, 393 mg (2.394 mmol) of 4-formyl-N-methylpyridine-2-carboxamide Example 42A were initially charged in 66 ml abs. tetrahydrofuran. At 0° C., 343 mg (2.873 mmol) of methylmagnesium bromide [1.4 mol in toluene/tetrahydrofuran 3/1] were added dropwise, and the reaction solution was stirred at this temperature for 1 h. 200 μl of semisaturated aqueous sodium bicarbonate solution and 200 ml of ethyl acetate were added to the reaction solution. The precipitate was filtered off and washed with ethyl acetate. The filtrate was evaporated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187428B2
Source datasetuspto-grants-2015_11
ORD IDord-825df3cf2f284e63927ca94387325f65
Source noteuspto-grants-2015_11