HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl chloroacetate → Potassium (Z)-2-chloro-1-ethoxy-3-oxoprop-1-en-1-olate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl chloroacetate | HCID 7751 | — |
| Reactant | Ethyl formate | HCID 8025 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Potassium (Z)-2-chloro-1-ethoxy-3-oxoprop-1-en-1-olate | HCID 86695681 | — |
Reaction Steps
A cooled (0° C.) suspension of ethyl 2-chloroacetate (17.47 ml, 163 mmol) and ethyl formate (13.18 ml, 163 mmol) in ether (250 ml) was treated slowly (over 3 hrs) with potassium 2-methylpropan-2-olate (18.31 g, 163 mmol) keeping the temperature below 5° C. The mixture was concentrated in vacuo and the resulting solid was washed with ether and dried (47° C. in a vacuum oven) to afford the title compound; 1H NMR (400 MHz, d6-DMSO) δ 8.95 (1H, s), 3.9 (2H, q), 1.1 (3H, t).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08883819B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-2edd4e26dd8645a1a80c47ee36006fe9 |
| Source note | uspto-grants-2014_11 |