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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750073Generated: November 1, 2026

Ethyl 3-(6-(4-(benzyloxy)butoxy)-2-pivalamidopyridin-3-yl)acrylate → Ethyl 3-(6-(4-(benzyloxy)butoxy)-2-pivalamidopyridin-3-yl)propanoate

https://huagongshe.com/reaction/1750073

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-(6-(4-(benzyloxy)butoxy)-2-pivalamidopyridin-3-yl)acrylateHCID 66632284—
CatalystNickelHCID 935—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 3-(6-(4-(benzyloxy)butoxy)-2-pivalamidopyridin-3-yl)propanoateHCID 6663131871.5%

Reaction Steps

Intermediate 8 (2.46 g, 5.4 mmol) was hydrogenated under an atmosphere of H2 (40 psi) using Raney Ni (1.59 g, 27.1 mmol) in THF (120 mL). The reaction was filtered to remove the Raney Ni and the filtrate was concentrated to afford ethyl 3-(6-(4-(benzyloxy)butoxy)-2-pivalamidopyridin-3-yl)propanoate (intermediate 9) (1.76 g, 71.5% crude) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156822B2
Source datasetuspto-grants-2015_10
ORD IDord-2aead0dd6e384353b5df1ad653362dd1
Source noteuspto-grants-2015_10