HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 67823864, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Diisopropyl Ether | HCID 7914 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Potassium | HCID 5462222 | — |
| Reactant | 1-(2,6-difluorophenyl)cyclopropanecarboxylic acid | HCID 14996288 | — |
| Reactant | Methyl 2-[2-(bromomethyl)phenyl]-3-methoxyprop-2-enoate | HCID 53395349 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 67823864 | HCID 67823864 | 86% |
Reaction Steps
A method similar to Example 1 was used and 12.8 g (65 mmol) of 1-(2,6-difluorophenyl)-cyclopropanecarboxylic acid, dissolved in 60 ml of ethanol, were converted with 4.0 g (71 mmol) of potassium hydroxide into the potassium salt of 2,6-difluorophenylcyclopropanecarboxylic acid, and said salt was then reacted, at 100° C., in 100 ml of N-methylpyrrolidone, with 11.4 g (40 mmol) of methyl alpha-(2-bromomethylphenyl)-betamethoxyacrylate. The resulting oily product was covered with a layer of diisopropyl ether and was crystallized by rubbing the wall of the vessel. Yield: 86%; mp.: 108°-110° C.; white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05371268 |
| Source dataset | uspto-grants-1994_12 |
| ORD ID | ord-ff4d71268dc14f64b7c8d62678655267 |
| Source note | uspto-grants-1994_12 |