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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1467049Generated: October 30, 2026

HCID 66746823, compound → HCID 66746696, compound

https://huagongshe.com/reaction/1467049

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 66746823HCID 66746823—
CatalystIronHCID 23925—
SolventEthyl AcetateHCID 8857—
SolventAcetic acid tetrahydrofuranHCID 23444217—
ProductHCID 66746696HCID 6674669683%

Reaction Steps

To a solution of 2-isobutoxy-6-nitrobenzonitrile (Example 41c, 34.3 g, 0.156 mol) in AcOH/THF (1:1 by volume, 250 mL) was added iron powder (17.36 g, 0.311 mol) in one portion. The stirred suspension was heated to reflux for 30 minutes. After it was cooled down to room temperature, the reaction solution was diluted with EtOAc (1 L). The solid was removed by filtration, and the filtrate was washed subsequently with water (300 mL×2), 1N NaOH (300 mL), saturated Na2CO3 aqueous solution (300 mL), brine (300 mL), and dried over Na2SO4. After evaporation of the solvent, the residue was purified by chromatography on silica gel eluting with 20% EtOAc in hexanes to give the title compound as a yellow oil (16.4 g, 83%). 1H NMR (400 MHz, DMSO-d6) δ 0.96 (d, J=6.8 Hz, 6H), 1.96-2.02 (m, 1H), 3.75 (d, J=6.4 Hz, 2H), 5.96 (s, 2H), 6.17 (d, J=8.4 Hz, 1H), 6.30 (d, J=8.4 Hz, 1H), 7.15 (t, J=8.8 Hz, 1H). MS 191 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09000054B2
Source datasetuspto-grants-2015_04
ORD IDord-82edec2b4cc04857ab4923d68d80aad6
Source noteuspto-grants-2015_04