HuagongsheHuagongshe Chemistry Print Report · For research reference only
Malonic Acid → 2-Chloro-4-(2-tetrahydropyranyloxy)cinnamic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Malonic Acid | HCID 867 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 2-Chloro-4-hydroxybenzaldehyde | HCID 185363 | — |
| Reactant | 2-Chloro-4-(tetrahydro-pyran-2-yloxy)-benzaldehyde | HCID 22137321 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 2-Chloro-4-(2-tetrahydropyranyloxy)cinnamic acid | HCID 54538134 | 55% |
Reaction Steps
Using 4.8 g of 2-chloro-4-(2-tetrahydropyranyloxy)benzaldehyde derived from 2-chloro-4-hydroxybenzaldehyde by the introduction of tetrahydropyranyl group thereinto, 4.2 g of malonic acid, 80 ml of pyridine, and 0.5 ml of piperidine, a reaction similar to that performed in Example 99 was carried out. As a result, 3.1 g of 2-chloro-4-(2-tetrahydropyranyloxy)cinnamic acid was obtained as crystal, which had the following physiochemical properties:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05344845 |
| Source dataset | uspto-grants-1994_09 |
| ORD ID | ord-3a7632feda264ccd8d81f8fbab9a9634 |
| Source note | uspto-grants-1994_09 |