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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 895715Generated: October 31, 2026

Ammonium Chloride → t-Butyl 5-amino-2-(6-cyano-2-naphthyloxy)benzoate

https://huagongshe.com/reaction/895715

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactantt-Butyl 2-(6-cyano-2-naphthyloxy)-5-nitrobenzoateHCID 22380917—
CatalystIronHCID 23925—
SolventWater ethanolHCID 19096565—
Productt-Butyl 5-amino-2-(6-cyano-2-naphthyloxy)benzoateHCID 22380961—

Reaction Steps

The compound (t-butyl 2-(6-cyano-2-naphthyloxy)-5-nitrobenzoate) (760 mg) obtained in a previous production example, iron powder (718 mg) and ammonium chloride (73 mg) were heated to reflux in ethanol:water (3:1, 30 ml) and reacted for 30 minutes. The insoluble portion was immediately filtered using celite, and the filtrate was concentrated. A saturated sodium bicarbonate solution was added to the obtained residue, and extraction was performed with ethyl acetate. The ethyl acetate layer was washed with saturated saline and then dried over magnesium sulfate, and the solvent was distilled off to obtain 736 mg of t-butyl 5-amino-2-(6-cyano-2-naphthyloxy)benzoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06916837B2
Source datasetuspto-grants-2005_07
ORD IDord-cba85a63da3e417ba2d78b997d74018d
Source noteuspto-grants-2005_07