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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1061848Generated: October 25, 2026

2-Bromo-6-methoxynaphthalene → (2-Fluoro-4-methoxyphenyl)(6-methoxy-2-naphthyl)methanol

https://huagongshe.com/reaction/1061848

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-6-methoxynaphthaleneHCID 78786—
Reactant2-Fluoro-4-methoxybenzaldehydeHCID 2734873—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product(2-Fluoro-4-methoxyphenyl)(6-methoxy-2-naphthyl)methanolHCID 222857011,953%

Reaction Conditions

Temperature-78 °C

Reaction Steps

n-Butyllithium (2.5 M, 16.9 mL) was added dropwise into a cold (−78° C.) solution of 2-bromo-6-methoxynaphthalene (10.0 g, 42.2 mmol), and THF (200 mL). The reaction mixture was stirred at −78° C. for 2 h, and then 2-fluoro-4-methoxybenzaldehyde (6.5 g, 42 2 mmol) in THF (10 mL) was added. The mixture was allowed to warm up to 0° C. stirred for 10 min, and then quenched with aqueous ammonium cholride. The mixture was poured into water, acidified with HCl (2N) and extracted with EtOAc. The organic extracts were dried over MgSO4. Evaporation and purification by flash chromatography (hexanes/EtOAc 3/1) gave a brown solid (12.2 g, 93% yield, m.p. 68-69° C.); MS m/e 312 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06960607B2
Source datasetuspto-grants-2005_11
ORD IDord-0176a36bd1764994a0db7dd75f3aa34d
Source noteuspto-grants-2005_11