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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 456436Generated: October 30, 2026

3-Fluoroanisole → 2-Bromo-3-fluoroanisole

https://huagongshe.com/reaction/456436

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-FluoroanisoleHCID 9975—
ReactantBromineHCID 24408—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product2-Bromo-3-fluoroanisoleHCID 2779318—

Reaction Conditions

Temperature-78 °C

Reaction Steps

The 3-fluoro anisole (15 g, 119 mmol) was placed in THF (300 mL) and cooled to about −78° C., and then n-BuLi (89 mL 1.6 M in hexanes) was added while maintaining the temperature at around −70° C. The mixture was stirred for about 15 minutes, and bromine (18.9 g, 119 mmol) was added over 10 minutes. The mixture was warmed to r.t. and stirred overnight. The mixture was quenched with water, diluted with ether (500 mL) and partitioned between water/ether (1/1 300 mL). The water layer was back extracted with ether (250 mL), and the combined organic fractions were dried, filtered and concentrated. The dark residue was distilled under house vacuum (product 115–130° C.) to recover about 13.8 g of the product as a gray oil (57%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07186715B2
Source datasetuspto-grants-2007_03
ORD IDord-5719310a41834985abbfe4ef4bda9c4d
Source noteuspto-grants-2007_03