HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetoacetate → HCID 23726010, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetoacetate | HCID 8868 | — |
| Reactant | 2-Chloro-4-fluorobenzaldehyde | HCID 145024 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | HCID 178484930 | HCID 178484930 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 23726010 | HCID 23726010 | — |
Reaction Steps
2 mmol N-methyl-1H-imidazol-2-formamidine methane sulfonate (Tommasi, R. A., Macchia, W. M., Parker, D. T., Tetrahedron Lett 1998, 39:5947-5950), 2 mmol 2-chloro-4-fluorobenzaldehyde, 2 mmol ethyl acetoacetate and 2.2 mmol sodium acetate were reacted under reflux in 10 ml anhydrous ethanol for 20 hr, concentrated, and then ethyl acetate and water were added to separate the layers. The ethyl acetate layer was dried over anhydrous sodium sulfate, and separated by a column chromatography to obtain 0.23 g of a yellowish columnar crystal with mp 166-167° C.; 1H-NMR (400 MHz, DMSO-d6) δ 1.03-1.06 (3H, m); 2.48 (3H, s); 3.81 (1H, s); 3.93-3.99 (2H, m); 6.00 (1H, s); 6.99-7.42 (5H, m); 9.57 (1H, s); MS (EI) 376.1 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08168642B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-a347bde053a04ed88726f47a80d88a2e |
| Source note | uspto-grants-2012_05 |