HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 456436Generated: October 30, 2026
3-Fluoroanisole → 2-Bromo-3-fluoroanisole
https://huagongshe.com/reaction/456436
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Fluoroanisole | HCID 9975 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Bromo-3-fluoroanisole | HCID 2779318 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07186715B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-5719310a41834985abbfe4ef4bda9c4d |
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| Source note | uspto-grants-2007_03 |
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