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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1663561Generated: October 30, 2026

Ethyl 3-(3-chlorophenyl)-4-nitrobutanoate → Ethyl 4-amino-3-(3-chlorophenyl)butanoate

https://huagongshe.com/reaction/1663561

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-(3-chlorophenyl)-4-nitrobutanoateHCID 22387109—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
ProductEthyl 4-amino-3-(3-chlorophenyl)butanoateHCID 2238706178%

Reaction Steps

In a 2 L pressure jar, under inert atmosphere, 196 g (733 mmoles) of ethyl 3-(3-chlorophenyl)-4-nitrobutanoate 377 are dissolved in 200 ml of ethanol. A suspension of 200 g of predried (3×, ethanol) Raney Nickel in 700 ml of ethanol is added and the mixture hydrogenated on a Parr hydrogenator at a maximum of 20 psi H2 pressure (STRONGLY EXOTHERMIC REACTION, ice/water cooling required). The mixture is degassed, filtered on a Celite/Norite pad, and the filtrate concentrated in vacuo, to give 136.7 g of crude 378, 78% yield, used as such in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08034958B2
Source datasetuspto-grants-2011_10
ORD IDord-53f6261992144e0dbc231eff4ecc1006
Source noteuspto-grants-2011_10