HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 471607Generated: October 27, 2026
Hydrogen Bromide → 2-Bromo-3-fluorobenzoic acid
https://huagongshe.com/reaction/471607
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | 2-Amino-3-fluorobenzoic acid | HCID 586408 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Catalyst | copper(I) bromide | HCID 24593 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Bromo-3-fluorobenzoic acid | HCID 302622 | 100% |
Reaction Steps
In a 1 L, three necked flask fitted with a dropping funnel and thermometer, were charged 2-amino-3-fluorobenzoic acid (20.0 g, 0.13 mol) and acetonitrile (160 mL). After cooling to 0° C., HBr (47%, 160 mL) was added drop wise over 10 min. To the resulting solution a solution of NaNO2 (10.0 g, 0.14 mol) in water (20.0 mL) was added drop wise over 1 h. After addition, the reaction mixture was stirred at 0° C. for 5 min, and copper(I) bromide (22.0 g, 0.15 mol) was added portionwise over 30 min. Stirring was continued at 70° C. in a an oil bath for 1 h. After cooling to 0° C., 700 mL of water was added and the precipitate was filtered, washed with cold water and dried under vacuum to give 28.23 g (100%) of the title compound as a white solid. The crude product was used in the next step without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08633186B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-b7e4cabab20244c384a9c5b988e858d5 |
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| Source note | uspto-grants-2014_01 |
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