HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 178471883, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Reactant | Cyclopropylamine | HCID 69828 | — |
| Reactant | Ethyl 2,4,6-trichloro-3,5-difluorobenzoylacetate | HCID 86589177 | — |
| Product | HCID 178471883 | HCID 178471883 | 74.8% |
Reaction Steps
82.9 g of ethyl 2,4,6-trichloro-3,5-difluorobenzoylacetate (0.25 mol), 66.6 g of triethyl orthoformate (0.45 mol) and 77.4 g of diacetyl oxide (0.72 mol) were stirred at 150° C. for 2.5 hours. Fractions having a lower boiling point were evaporated under reduced pressure. To the residue was added 250 ml of anhydrous ethanol. 14.5 g of cyclopropylamine (0.25 mol) was added to the solution under cooling of ice water and the reaction was then carried at room temperature for 2 hours. The resultant mixture was filtered under suction. The residue was re-crystallized from a mixture of petroleum ether and cyclohexane to yield 74.5 g (0.187 mol) of ethyl 2-(2,4,6-trichloro-3,5-difluorobenzoyl)-3-cyclopropylaminoacrylate in 74.6% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06699992B2 |
| Source dataset | uspto-grants-2004_03 |
| ORD ID | ord-b89926daf4454c288be859258652d887 |
| Source note | uspto-grants-2004_03 |