HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 23044435, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethanol, 1-ethoxy-2,2,2-trifluoro- | HCID 9897 | — |
| Reactant | Methyl isocyanoacetate | HCID 547815 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 23044435 | HCID 23044435 | — |
Reaction Steps
To a solution of methyl isocyanoacetate (4.55 ml) and triethylamine (7.0 ml) in benzene (45 ml) was added trifluoroacetaldehyde ethyl hemiacetal (8 ml) at 0° C. The mixture was stirred at room temperature for an hour and then heated with reflux for 2 hours. The resulting mixture was neutrized with acetic acid, evaporated, diluted with ethyl acetate and washed successively with water (2 times), 10% aqueous sodium hydrogen carbonate and brine. After drying over sodium sulfate, the ethyl acetate extract was filtered and concentrated. The residue was distilled (60° C. /4 mmHg) to give 4-methoxycarbonyl-5-trifluoromethyl-2-oxazoline (5 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04939241 |
| Source dataset | uspto-grants-1990_07 |
| ORD ID | ord-7dfb1978bb984aabb5e59bf7776b5ba8 |
| Source note | uspto-grants-1990_07 |