HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chlorobenzaldehyde → HCID 13564978, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chlorobenzaldehyde | HCID 6996 | — |
| Reactant | 2-Propanone, 1-nitro- | HCID 66296 | — |
| Reactant | HCID 21278157 | HCID 21278157 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 13564978 | HCID 13564978 | — |
Reaction Steps
28.1 g (200 mmol) of 2-chlorobenzaldehyde are boiled under reflux with 37.4 g (200 mmol) of 2-acetoxyethyl β-aminocrotonate and 32.6 g (320 mmol) of nitroacetone in 400 ml of ethanol for 4 hours. The mixture is cooled and concentrated. The evaporation residue is taken up in ethyl acetate and the mixture is washed with water, sodium bicarbonate solution and water again, dried and concentrated. The semi-solid evaporation residue is stirred with ethanol, filtered off with suction and washed with ethanol. 23.2 g (29.4% of theory) of a yellow-colored product of melting point 158°-160° C. are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04645775 |
| Source dataset | uspto-grants-1987_02 |
| ORD ID | ord-09dfd876ef0a4019949835f7b55cc85e |
| Source note | uspto-grants-1987_02 |