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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 219561Generated: October 31, 2026

Tert-butyl 3-(4-cyano-3-methylphenyl)acrylate → Tert-butyl 3-(4-cyano-3-methylphenyl)propanoate

https://huagongshe.com/reaction/219561

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 3-(4-cyano-3-methylphenyl)acrylateHCID 68649265—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl 3-(4-cyano-3-methylphenyl)propanoateHCID 6864934498%

Reaction Steps

To a solution of tert-butyl 3-(4-cyano-3-methylphenyl)acrylate obtained in step 1, (5.3 g) in ethyl acetate (50 mL) was added palladium on carbon (500 mg) and the mixture was placed under a pressure of 3 kg of hydrogen for 3 h at RT. The catalyst was removed by filtration and the filtrate was concentrated under vacuum to afford the title compound as white solid (5.2 g, 98%). 1H-NMR (CDCl3, 400 MHz) δ 7.51-7.53 (1H, d), 7.16 (1H, s), 7.10-7.12 (1H, d), 2.91-2.94 (2H, t), 2.53-2.57 (2H, t), 2.52 (3H, s), 1.42 (9H, s). LC/MS: 246.0 (M+H)+. HPLC (Method C) Rt 3.23 min (Purity: 96.2%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202856B2
Source datasetuspto-grants-2012_06
ORD IDord-b829134f99034e71943095a307e96f0d
Source noteuspto-grants-2012_06