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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1259496Generated: November 2, 2026

Sodium Bicarbonate → 2-Amino-4-(benzyloxy)-3-methoxybenzonitrile

https://huagongshe.com/reaction/1259496

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant4-(Benzyloxy)-3-methoxy-2-nitrobenzonitrileHCID 58219845—
CatalystIronHCID 23925—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventSodium chloride; waterHCID 57417360—
Product2-Amino-4-(benzyloxy)-3-methoxybenzonitrileHCID 5821984988%

Reaction Steps

A degassed solution of 4-(benzyloxy)-3-methoxy-2-nitrobenzonitrile (185 g, 651 mmol) in glacial acetic acid (3500 mL) and water (10 mL) was cooled to 5° C. and treated with iron powder (182 g, 3.25 mol). After 3 days the reaction mixture was filtered through Celite, and the filtrate concentrated under reduced pressure. The oil, thus obtained, was treated with brine, neutralized with a sodium bicarbonate solution and extracted into DCM. The resulting emulsion was filtered through Celite after which the organic layer was separated, washed with brine, dried (sodium sulfate) and concentrated under reduced pressure to afford the title compound as a solid (145 g, 88%): 1H NMR (DMSO-d6) δ: 7.32-7.44 (5H, m), 7.15 (1H, d), 6.47 (1H, d), 5.69 (2H, s), 5.15 (2H, s), 3.68 (3H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466283B2
Source datasetuspto-grants-2013_06
ORD IDord-3127113d63ec40649fd2ef0f36c1415e
Source noteuspto-grants-2013_06