HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chlorobenzaldehyde → HCID 54543583, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chlorobenzaldehyde | HCID 6996 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | HCID 15428861 | HCID 15428861 | — |
| Catalyst | Piperidine, acetate | HCID 9793820 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 54543583 | HCID 54543583 | 97% |
Reaction Steps
16.64 g (0.118 mole) of 2-chloro-benzaldehyde (V) and 24.7 g (0.118 mole) of ethyl-4-(2-chloroethoxy)-acetoacetate (IV) are reacted in 365 ml of isopropanol in the presence of a piperidine acetate catalyst [10 g (11.8 millimoles) of piperidine+0.7 g (11.8 millimoles) of acetic acid] at room temperature for 10 hours. The reaction mixture is evaporated, the residual oil is dissolved in dichloro methane, washed with water and dried. The organic phase is evaporated in vacuo. Thus 37.9 g of the desired product are obtained in the form of a yellow oil, yield 97%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06046337 |
| Source dataset | uspto-grants-2000_04 |
| ORD ID | ord-8f53d5c582bb4f5aab61dedae0a15b06 |
| Source note | uspto-grants-2000_04 |