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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1820950Generated: November 1, 2026

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

https://huagongshe.com/reaction/1820950

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 6864934499.7%

Reaction Steps

A mixture of 5.0 g (20.6 mmol) of tert-butyl 3-(3-methyl-4-cyanophenyl)acrylate (from Step A) and 500 mg of 10% palladium on carbon in 200 mL of EtOAc was stirred under 1 atm of hydrogen at rt for 16 h. The catalyst was removed by filtration. The filtrate was concentrated to afford 5.04 g of the title compound: 1H NMR (500 MHz, CDCl3) δ 1.42 (s, 9H), 2.53 (s, 3H), 2.55 (t, J=7.6, 2H), 2.93 (t, J=7.6, 2H), 7.12 (d, J=7.8, 1H), 7.17 (s, 1H), 7.51 (d, J=7.8, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07605171B2
Source datasetuspto-grants-2009_10
ORD IDord-9cfdcf026cbd4f3a968ea66a32477831
Source noteuspto-grants-2009_10