HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 4-aminocyclohexanecarboxylate → Ethyl 4-(4-acetoxy-3-methoxycinnamamido)-1-cyclohexanecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 4-aminocyclohexanecarboxylate | HCID 409963 | — |
| Reactant | 4-Acetoxy-3-methoxycinnamoyl chloride | HCID 54468022 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | Ethyl 4-(4-acetoxy-3-methoxycinnamamido)-1-cyclohexanecarboxylate | HCID 53918885 | 60.2% |
Reaction Steps
Using 2.5 g of 4-acetoxy-3-methoxycinnamoyl chloride, 3.7 g of ethyl 4-amino-1-cyclohexanecarboxylate described in the literature [V. Skaric, M. Kovacevic, and D. Skaric, J. Chem. Soc. Perkin I, 1199-1201 (1976)], and 100 ml of pyridine, a reaction similar to that conducted in Example 53 was carried out. As a result, 2.3 g of ethyl 4-(4-acetoxy-3-methoxycinnamamido)-1-cyclohexanecarboxylate (a compound of the present invention) was obtained as pale yellowish white 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-6ac29d7785e14453afe36451965d392d |
| Source note | uspto-grants-1994_09 |