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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 462551Generated: November 2, 2026

Iodoethane → N-ethyl-2,6-dimethoxy-4-(methoxy-carbonyl)carbanilic acid benzyl ester

https://huagongshe.com/reaction/462551

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantSodium hydrideHCID 24758—
Reactant2,6-Dimethoxy-4-(methoxy-carbonyl)-carbanilic acid benzyl esterHCID 54226013—
SolventDimethylformamideHCID 6228—
ProductN-ethyl-2,6-dimethoxy-4-(methoxy-carbonyl)carbanilic acid benzyl esterHCID 53836153—

Reaction Steps

A suspension of 103 g. of 2,6-dimethoxy-4-(methoxy-carbonyl)-carbanilic acid benzyl ester and 17.3 g. of sodium hydride (50% dispersion in oil) in 1 liter of absolute dimethylformamide was stirred at room temperature for 4 hours and subsequently treated with 56.2 g. of ethyl iodide with stirring and ice-cooling. After stirring at room temperature for 30 minutes, the dimethylformamide was removed at 60° C. under vacuum. Then, 1 liter of water was added to the residue and the mixture was extracted with two 1.5 liter portions of ethyl acetate. The ethyl acetate extract was washed with two 700 ml. portions of water, dried over magnesium sulfate and evaporated under vacuum. After recrystallization of the residue from alcohol, there was obtained N-ethyl-2,6-dimethoxy-4-(methoxy-carbonyl)-carbanilic acid benzyl ester having a melting point of 85°-86° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04515948
Source datasetuspto-grants-1985_05
ORD IDord-0d840fd243a04e54bcb6c25c1a969570
Source noteuspto-grants-1985_05