HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 2-Ethoxymethylene-1-(2-nitro-4-trifluoromethylphenyl)butan-1,3-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Reactant | 1-(2-Nitro-4-trifluoromethylphenyl)-butan-1,3-dione | HCID 54014622 | — |
| Product | 2-Ethoxymethylene-1-(2-nitro-4-trifluoromethylphenyl)butan-1,3-dione | HCID 53751742 | — |
Reaction Steps
A mixture of 1-(2-nitro-4-trifluoromethylphenyl)-butan-1,3-dione (-11.0 g), triethyl orthoformate (11.3 g) and acetic anhydride (12.3 g) was stirred and heated at reflux for 3 hours. After cooling, the mixture was evaporated to dryness. Toluene (50 ml) was added and the mixture was evaporated to dryness to give 2-ethoxymethylene-1-(2-nitro-4-trifluoromethylphenyl)-butan-1,3-dione as a crude brown oil which was not further purified.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05859283 |
| Source dataset | uspto-grants-1999_01 |
| ORD ID | ord-661bdaa1897f4e9a8ec38002ff25ab30 |
| Source note | uspto-grants-1999_01 |