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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2105743Generated: November 1, 2026

Water → 2-Bromo-7-methylnaphthalene

https://huagongshe.com/reaction/2105743

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
Reactant2,7-DibromonaphthaleneHCID 625355—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
Product2-Bromo-7-methylnaphthaleneHCID 15321336—

Reaction Conditions

Temperature-30 °C

Reaction Steps

Suspension of 2,7-dibromonaphthalene (61.4 g, 0.21 mole) in ether (400 ml) was cooled to −30° C., and n-BuLi (1.6M in hexane, 135 ml, 0.21 mole) was added. Reaction mixture was allowed to warm to room temperature, stirred for additional 2.5 h, cooled to −30° C., and CH3I (13.5 ml, 0.21 mole) was added. Reaction mixture was allowed to warm to room temperature, stirred for additional 16 h, treated by water (100 ml). Organic layer was separated, water layer was extracted by ether (6×100 ml). Combined organic fraction was evaporated, giving practically pure solid product. The yield 38.1 g (82%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07579417B2
Source datasetuspto-grants-2009_08
ORD IDord-c12bf8f98e7244df944c14f575aac230
Source noteuspto-grants-2009_08