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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1275928Generated: October 29, 2026

Acetic Acid → n-(1-Ethoxy)cyclopropyl-3,4-difluoro-2-methoxyaniline

https://huagongshe.com/reaction/1275928

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant(1-Ethoxycyclopropoxy)trimethylsilaneHCID 2734686—
Reactant3,4-Difluoro-2-methoxyanilineHCID 11137425—
SolventEthanolHCID 702—
Productn-(1-Ethoxy)cyclopropyl-3,4-difluoro-2-methoxyanilineHCID 8802237283%

Reaction Steps

Into a 200-ml four-necked flask provided with a reflux condenser, a thermometer and a stirrer were fed 7.96 g (0.05 mol) of 3,4-difluoro-2-methoxyaniline, 40 g (0.67 mol) of acetic acid and 100 ml of ethanol. To the resulting mixture being stirred at room temperature was dropwise added 9.24 g (0.053 mol) of 1-ethoxy-1-trimethylsilyloxycyclopropane. The resulting mixture was placed on an oil bath and refluxed at 80° C. for 3 hours with stirring, in a nitrogen current. The resulting reaction mixture was concentrated under aspirator vacuum by the use of a rotary evaporator. Lastly, the acetic acid remaining in the resulting residue was removed by the use of a vacuum pump to obtain 11.5 g of an oily substance. This oily substance was subjected to vacuum distillation to obtain 10.1 g (yield: 83.0%) of N-(1-ethoxy)cyclopropyl-3,4-difluoro-2-methoxyaniline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06162944
Source datasetuspto-grants-2000_12
ORD IDord-eb7be823d3ae4ae0916a96df4c1dcda2
Source noteuspto-grants-2000_12