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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | (1-Ethoxycyclopropoxy)trimethylsilane | HCID 2734686 | — |
| Reactant | 3,4-Difluoro-2-methoxyaniline | HCID 11137425 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | n-(1-Ethoxy)cyclopropyl-3,4-difluoro-2-methoxyaniline | HCID 88022372 | 83% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06162944 |
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| Source dataset | uspto-grants-2000_12 |
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| ORD ID | ord-eb7be823d3ae4ae0916a96df4c1dcda2 |
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| Source note | uspto-grants-2000_12 |
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