HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethoxalyl chloride → Ethyl [(3-chloro-2,6-difluorophenyl)carbamoyl]formate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethoxalyl chloride | HCID 20884 | — |
| Reactant | 3-Chloro-2,6-difluoroaniline | HCID 17750745 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl [(3-chloro-2,6-difluorophenyl)carbamoyl]formate | HCID 123515043 | 72% |
Reaction Steps
To a solution of 3-chloro-2,6-difluoroaniline (430 mg, 2.55 mmol) and TEA (0.5 mL, 3.59 mmol) in THF (5 mL) was added ethyl 2-chloro-2-oxoacetate (0.3 mL, 2.63 mmol). A white precipitate was formed immediately. After 30 min, the reaction mixture was filtered and rinsed with ether. The filtrate was concentrated to yield a crude yellow oil, which was purified by silica gel chromatography to yield the desired product (484 mg, 72%) as a white solid. 1H NMR (500 MHz, CDCl3) δ 8.42 (br. s., 1H), 7.35 (m, 1H), 6.98 (m, 1H), 4.45 (q, J=7.2 Hz, 2H), 1.45 (t, J=7.2 Hz, 3H). MS (ESI) m/z: 263.9 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08901115B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-468de7c5843d466189b4ee58e640f275 |
| Source note | uspto-grants-2014_12 |