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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 43832Generated: October 29, 2026

Ethyl 3-(4-tert-butoxycarbonylaminocyclohex-1-enyl)benzoate → Ethyl 3-(4-aminocyclohex-1-enyl)benzoate

https://huagongshe.com/reaction/43832

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-(4-tert-butoxycarbonylaminocyclohex-1-enyl)benzoateHCID 67548489—
Solvent1,4-Dioxane hydrochlorideHCID 20443148—
ProductEthyl 3-(4-aminocyclohex-1-enyl)benzoateHCID 6754930357.8%

Reaction Steps

A 4 N hydrochloric acid/1,4-dioxane solution (20 mL) was added to ethyl 3-(4-tert-butoxycarbonylaminocyclohex-1-enyl)benzoate obtained in Example (195b) (510 mg, 1.48 mmol). The mixture was stirred at room temperature for one hour, and the solvent was evaporated under reduced pressure. The resulting residue was dissolved in methanol. Amberlite IRA-400(Cl) ion exchange resin (20 g) was added, and the mixture was stirred at room temperature for one hour. Amberlite was filtered off, and then the solution was concentrated under reduced pressure to obtain 210 mg of the title compound as a colorless oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536197B2
Source datasetuspto-grants-2013_09
ORD IDord-bf23ea28f6034bdda8416854eaad78ca
Source noteuspto-grants-2013_09