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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1035608Generated: October 29, 2026

3-Bromo-7-methoxy-1-naphthonitrile → 7-Methoxy-3-(3-methoxyphenyl)-1-naphthonitrile

https://huagongshe.com/reaction/1035608

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromo-7-methoxy-1-naphthonitrileHCID 11470997—
Reactant3-Methoxyphenylboric acidHCID 22173823—
Product7-Methoxy-3-(3-methoxyphenyl)-1-naphthonitrileHCID 5944347753%

Reaction Steps

The compound is prepared by the reaction of 3-bromo-7-methoxy-1-naphthonitrile (1.4 g, 1.76 mmol, 1 eq) with 3-methoxyphenylboric acid (320 mg, 2.11 mmol, 1.2 eq) according to method A in 24 h. Purification by column chromatography with hexane/ethyl acetate 9/1 as the eluent yielded the desired compound in a yield of 53%, 300 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546392B2
Source datasetuspto-grants-2013_10
ORD IDord-d2964a9e2051423a9f62e9574ec4a7dc
Source noteuspto-grants-2013_10