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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2225510Generated: October 27, 2026

Ethyl 4-aminocyclohexanecarboxylate → Ethyl 4-(4-acetoxy-3-methoxycinnamamido)-1-cyclohexanecarboxylate

https://huagongshe.com/reaction/2225510

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-aminocyclohexanecarboxylateHCID 409963—
Reactant4-Acetoxy-3-methoxycinnamoyl chlorideHCID 54468022—
SolventPyridineHCID 1049—
ProductEthyl 4-(4-acetoxy-3-methoxycinnamamido)-1-cyclohexanecarboxylateHCID 5391888560.2%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05344845
Source datasetuspto-grants-1994_09
ORD IDord-6ac29d7785e14453afe36451965d392d
Source noteuspto-grants-1994_09