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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727439Generated: October 29, 2026

HCID 67417282, compound → HCID 67416470, compound

https://huagongshe.com/reaction/1727439

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67417282HCID 67417282—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 67416470HCID 67416470120.4%

Reaction Steps

A mixture of 2-(nitro-1,3-dioxoisoindolin-2-yl)-2-(3-ethoxy-4-methoxyphenyl)ethanenitrile (3.9 g, 7.8 mmol) and 10% Pd/C (0.6 g) in methanol (150 mL) was hydrogenated at 50 psi for 3 hours. The mixture was filtered through celite, and the celite was washed with methylene chloride. The filtrate was concentrated and the residue was purified by chromatography (SiO2, CH2Cl2:CH3OH 95:5) to give 3.3 g (91%) of 2-(4-amino-1,3-dioxoisoindolin-2-yl)-2-(3-ethoxy-4-methoxyphenyl)ethanenitrile; 1H NMR (DMSO-d6) δ 7.50-7.43 (dd, J=7.3 and 8.3 Hz, 1H), 7.03-6.91 (m, 5H), 6.55 (s, 2H), 5.55-5.48 (dd, J=6.6 and 9.9 Hz, 1H), 3.99 (q, J=7.0 Hz, 2H), 3.72 (s, 3H), 3.76-3.48 (m, 2H), 1.31 (t, J=7 Hz, 3H); 13C NMR (DMSO-d6) δ 168.81, 167.59, 148.88 146.82, 135.55, 131.56, 129.70, 121.86, 121.80, 119.27, 118.26, 112.10, 111.82, 111.06, 63.82, 55.48, 49.46, 20.54, 14.61.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07495112B2
Source datasetuspto-grants-2009_02
ORD IDord-22fb9202b50248afad61d8a038e19f3d
Source noteuspto-grants-2009_02