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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2225725Generated: November 2, 2026

Sodium hydride → alpha-Oxo-4-[4-(4-pyridinyl)butoxy]benzeneacetic acid methyl ester

https://huagongshe.com/reaction/2225725

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantMethanesulfonateHCID 85257—
Reactant4-PyridinebutanolHCID 2784655—
ReactantBenzeneacetic acid, 4-hydroxy-alpha-oxo-, methyl esterHCID 3084696—
CatalystAcetic AcidHCID 176—
SolventDimethylformamideHCID 6228—
Productalpha-Oxo-4-[4-(4-pyridinyl)butoxy]benzeneacetic acid methyl esterHCID 5448686730.9%

Reaction Conditions

Temperature60 °C

Reaction Steps

A stirred mixture of 4-hydroxy-alpha-oxobenzeneacetic acid methyl ester (1.086 g) in dimethylformamide (10 mL) under argon was treated with 55% sodium hydride (0.261 g), stirred for 15 minutes and treated with the mesylate prepared from 0.906 g of 4-pyridinebutanol. The mixture was heated under argon at 60° C. for 4 hours. The cooled mixture was treated with glacial acetic acid (2 drops) and the volatiles were removed under vacuum. The residue was mixed with dichloromethane and dilute cold sodium bicarbonate solution. The dichloromethane extracts were dried (Na2SO4), filtered, and evaporated to give crude product. The material was purified by HPLC (hexane-acetone; 2: 1) to provide 0.58 g of alpha-oxo-4-[4-(4-pyridinyl)butoxy]benzeneacetic acid methyl ester as a colorless oil whose NMR was compatible with the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05344843
Source datasetuspto-grants-1994_09
ORD IDord-63c69b63f3084e8888618e258be1d907
Source noteuspto-grants-1994_09