HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 727835Generated: October 27, 2026
Triethyloxonium tetrafluoroborate → 1-ethoxy-2-(2,6-difluorophenyl)-1-(N-methylimino)-ethane
https://huagongshe.com/reaction/727835
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethyloxonium tetrafluoroborate | HCID 2723982 | — |
| Reactant | 2,6-Difluorophenylacetic acid methylamide | HCID 54384531 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-ethoxy-2-(2,6-difluorophenyl)-1-(N-methylimino)-ethane | HCID 19904232 | — |
Reaction Steps
5.55 g (30 mmol) of 2,6-difluorophenylacetic acid methylamide are dissolved in 70 ml of dichloromethane, 7.4 g (39 mmol) of triethyloxonium tetrafluoroborate are added thereto and the whole is stirred for 25 hours at room temperature. The reaction mixture is then extracted by shaking in succession with cold 2N sodium carbonate solution, ice-water and cold saturated sodium chloride solution, dried over magnesium sulphate and concentrated. A mixture of ether and hexane is added to the residue, the unreacted educt remaining undissolved and being filtered off. The filtrate is concentrated and subjected to distillation in a bulb tube. 4 g (62.6% of the theoretical yield) of 1-ethoxy-2-(2,6-difluorophenyl)-1-(N-methylimino)-ethane which boils at 70° (0.02 mm) are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05045556 |
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| Source dataset | uspto-grants-1991_09 |
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| ORD ID | ord-a9d73528f0974c99b0daa21dc23db04a |
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| Source note | uspto-grants-1991_09 |
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