HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl acetoacetate → HCID 24810449, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl acetoacetate | HCID 7757 | — |
| Reactant | 2-Chloro-4-fluorobenzaldehyde | HCID 145024 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 2,6-Difluorobenzamidine hydrochloride | HCID 46318424 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 24810449 | HCID 24810449 | 26.6% |
Reaction Steps
2 mmol 2,6-Difluorobenzamidine hydrochloride (Boere, R. J., Oakley, R. T., Read, R. V., J. Organometal. Chem. 1987, 331:161-167), 2 mmol 2-chloro-4-fluorobenzaldehyde, 2 mmol methyl 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 0.21 g of a colorless fine needle crystal with mp 126-128° C.; 1H-NMR (400 MHz, DMSO-d6) δ 2.87 (3H, s); 3.45 (3H, s); 5.92 (1H, s); 7.10-7.38 (6H, m); 9.87 (1H, s); MS (EI) 394.0 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08168642B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-f15f158254ff4aa88de3e32271820ef2 |
| Source note | uspto-grants-2012_05 |