HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chlorobenzaldehyde → HCID 54282972, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chlorobenzaldehyde | HCID 6996 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | HCID 15428864 | HCID 15428864 | — |
| Catalyst | Piperidine, acetate | HCID 9793820 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 54282972 | HCID 54282972 | 83% |
Reaction Steps
10 g (33 millimoles) of ethyl-4-(2-iodoethoxy)-acetoacetate (XIII) and 4.64 g (33 millimoles) of 2-chloro-benzaldehyde (V) are reacted in 100 ml of isopropanol in the presence of a piperidine acetate catalyst [0.28 g (3.3 millimoles) of piperidine+0.198 g (3.3 millimoles) of acetic acid] at room temperature for 10 hours. The reaction mixture is evaporated, the residual oil dissolved in dichloro methane, washed with water and dried. The organic phase is evaporated in vacuo. Thus 11.55 g of the desired product are obtained in the form of a reddish brown oil, yield 83%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06046337 |
| Source dataset | uspto-grants-2000_04 |
| ORD ID | ord-b7f453c806044400ada821e59cc902a5 |
| Source note | uspto-grants-2000_04 |