HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Methyl 4,4-difluoro-3-oxo-2-(morpholin-4-ylmethylidene)butyrate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl 3-morpholin-4-ylacrylate | HCID 351261 | — |
| Reactant | 2,2-Difluoroacetyl fluoride | HCID 2778914 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Methyl 4,4-difluoro-3-oxo-2-(morpholin-4-ylmethylidene)butyrate | HCID 86651360 | 82% |
Reaction Conditions
| Temperature | -30 °C |
|---|
Reaction Steps
Methyl 3-morpholin-4-ylacrylate (96.3%, 8.5 g, 50 mmol) and triethylamine (5.2 g, 50 mmol) were initially charged in toluene (250 ml) and cooled to −30° C. At this temperature, difluoroacetyl fluoride (5.0 g, 50 mmol) was introduced. The reaction mixture was stirred at −30° C. for 3 h and then, over a period of 1 hour, warmed to room temperature. Under reduced pressure, the reaction mixture was freed from the solvent. The residue obtained was 15.5 g of an orange solid which, according to quant. 1H-NMR, consisted to 66.4% of methyl 4,4-difluoro-3-oxo-2-(morpholin-4-ylmethylidene)butyrate (yield: 82%). 1H-NMR (CDCl3): δ=3.4 (m, 2H), 3.7 (m, 2H), 3.75 (s, 3H), 3.85 (m, 2H), 6.6 (t, 1H), 7.85 ppm (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08592578B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-db2d23c6f86e41c4a3fcce0c1f40d866 |
| Source note | uspto-grants-2013_11 |