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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2410165Generated: October 31, 2026

Ethyl Acetate → HCID 66745877, compound

https://huagongshe.com/reaction/2410165

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantHCID 66747182HCID 66747182—
CatalystIronHCID 23925—
SolventAcetic acid tetrahydrofuranHCID 23444217—
ProductHCID 66745877HCID 66745877104%

Reaction Steps

To a solution of 2-(cyclohexyloxy)-6-nitrobenzonitrile (Example Hc, 50.0 g, 0.20 mol) in THF/AcOH (1:1 by volume, 500 mL) was added iron powder (34.0 g, 0.61 mol) in one portion at room temperature under nitrogen. The reaction mixture was refluxed for 40 min under nitrogen and cooled down to room temperature and EtOAc (2 L) was added. The precipitate that formed was filtered off and washed with EtOAc. The organic layer was separated and washed successively with water (2×300 mL), aqueous NaOH (1.0 N, 2×300 mL), saturated Na2CO3 solution (300 mL), brine (300 mL), dried over Na2SO4 filtered and evaporated under reduced pressure. The residue was purified by chromatography on silica gel eluting with 25% EtOAc in hexanes to give 2-amino-6-(cyclohexyloxy)benzonitrile as a pale yellow oil (45.0 g, 94%), which solidified after storage overnight at room temperature.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08815956B2
Source datasetuspto-grants-2014_08
ORD IDord-ed0ac44e60684a8d99734488eb9982af
Source noteuspto-grants-2014_08