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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339350Generated: October 25, 2026

Ethanol → N-(heptan-4-yl)-4-(2-methoxyethoxy)-3-methylbenzamide

https://huagongshe.com/reaction/339350

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPotassium HydroxideHCID 14797—
Reactant1-Chloroethan-1-olHCID 12639035—
Reactant4-hydroxy-3-methyl-N-(1-propyl-butyl)-benzamideHCID 57527768—
ProductN-(heptan-4-yl)-4-(2-methoxyethoxy)-3-methylbenzamideHCID 5752790639%

Reaction Conditions

Temperature80 °C

Reaction Steps

Potassium hydroxide (4 mmol) was dissolved in ethanol (5 mL) and heated at 80° C. 4-hydroxy-3-methyl-N-(1-propyl-butyl)-benzamide (example 58) (1 mmol) was added into the solution followed by chloroethanol (3 mmol). The reaction was stirred overnight at 80° C. The reaction mixture was concentrated down and dissolved in 5% citric acid. The mixture was stirred for 1 hour. The aqueous mixture was extracted three times with ethyl acetate. The combined ethyl acetate was washed with water and dried down over sodium sulfate. The organic layer was concentrated down and purified by HPLC to yield 39% of N-(heptan-4-yl)-4-(2-methoxyethoxy)-3-methylbenzamide. MS (M+H, 308.25).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895050B2
Source datasetuspto-grants-2014_11
ORD IDord-57afbe97652f466dbe71c191c0288561
Source noteuspto-grants-2014_11