HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1497953Generated: October 30, 2026
3-Bromo-2-fluorobenzonitrile → 3-Bromo-2-tert-butoxy-benzonitrile
https://huagongshe.com/reaction/1497953
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Bromo-2-fluorobenzonitrile | HCID 2761200 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Bromo-2-tert-butoxy-benzonitrile | HCID 58270661 | — |
Reaction Steps
A mixture of 3-bromo-2-fluoro-benzonitrile (40.0 g, 0.200 mol) and tetrahydrofuran (200 mL) was chilled to 0° C. and stirred for 5 min. A solution of potassium tert-butoxide (130 mL, 0.210 mol) was added dropwise at 0° C. and the reaction was allowed to warm to RT with stirring over 90 min. The reaction was quenched with water (200 mL) and 2 M Na2CO3 (100 mL) and extracted with EtOAc (3×200 mL). The organic layer was dried over Na2SO4 and the solvent was removed by rotary evaporation to provide the title compound as a light yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09199993B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-65518a24373f4c69aefa624b3b2e1c0f |
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| Source note | uspto-grants-2015_12 |
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