HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl chloroacetate → Potassium 2-chloro-3-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 | — |
| Product | Potassium 2-chloro-3-ethoxy-3-oxoprop-1-en-1-olate | HCID 74089075 | 67.3% |
Reaction Steps
To a suspension of potassium tert-butoxide (5.2 g) in IPE (50 mL) were added ethyl 2-chloroacetate (5.6 g) and ethyl formate (3.4 g) under ice-cooling, and the mixture was stirred overnight at room temperature. The precipitate was collected by filtration, and dried to give the title compound (5.8 g). 1H NMR (300 MHz, DMSO-d6) δ 1.11 (3H, t, J=7.2 Hz), 3.92 (2H, q, J=7.2 Hz), 8.95 (1H, brs).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09296746B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-ffb6d8f60a62411da880ef68c9c7a295 |
| Source note | uspto-grants-2016_03 |