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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 536212Generated: October 30, 2026

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

https://huagongshe.com/reaction/536212

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 (Step 4, 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 numberUS08859572B2
Source datasetuspto-grants-2014_10
ORD IDord-988ba0ed200748eda629f86f96308ad1
Source noteuspto-grants-2014_10