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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 895712Generated: October 27, 2026

Water → t-Butyl 2-(6-cyano-2-naphthyloxy)-5-nitrobenzoate

https://huagongshe.com/reaction/895712

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant6-Hydroxy-2-naphthonitrileHCID 4589476—
ReactantTert-butyl 2-fluoro-5-nitrobenzoateHCID 22380964—
SolventDimethylformamideHCID 6228—
Productt-Butyl 2-(6-cyano-2-naphthyloxy)-5-nitrobenzoateHCID 22380917—

Reaction Steps

The compound (t-butyl 2-fluoro-5-nitrobenzoate) (1.74 g) obtained in a previous production example, 6-cyano-2-naphthol (1.86 g) and potassium carbonate (8.2 g) were heated to 50° C. in N,N-dimethylformamide and reacted for 2 hours. After cooling to room temperature, water was added and extraction was performed with ethyl acetate. The ethyl acetate layer was washed with saturated saline and dried over magnesium sulfate, and the solvent was distilled off. The residue was purified by silica gel chromatography (300 g, hexane:ethyl acetate=5:1) to obtain 3.23 g of t-butyl 2-(6-cyano-2-naphthyloxy)-5-nitrobenzoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06916837B2
Source datasetuspto-grants-2005_07
ORD IDord-963d3e736c7340afb56855abd981d7af
Source noteuspto-grants-2005_07