HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6968Generated: October 26, 2026
Hydrogen Bromide → 2-Bromo-4-chlorobenzoic acid
https://huagongshe.com/reaction/6968
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Sodium Nitrate | HCID 24268 | — |
| Reactant | 2-Amino-4-chlorobenzoic acid | HCID 66646 | — |
| Catalyst | Copper bromide (CuBr2) | HCID 24611 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Bromo-4-chlorobenzoic acid | HCID 33126 | 59% |
Reaction Steps
An aqueous solution of sodium nitrate (2.21 g) in water (15 mL) is added dropwise to a stirred, ice-cooled mixture of 2-amino-4-chlorobenzoic acid (5.00 g, 29.1 mmol) and 48% hydrobromic acid (150 mL) in water (150 mL). The resultant mixture is stirred for 2 hr at 0° C. Then it is treated dropwise with an aqueous solution of copper bromide (7.81 g) in water (20 mL). Upon the completion of the addition, the reaction mixture is allowed to warm to ambient temperature where it is stirred overnight. After extraction with ethyl acetate/hexanes (3:1; 2×400 mL), the combined organic layers are washed with brine (200 mL), dried, concentrated, and chromatographed on silica (1% methyl alcohol and 0.5% acetic acid in chloroform) to give the title compound (4.04 g, 59% yield). mp 154–155° C.; ES(−)MS m/z 233, (M−H)− consistent with 1 Br an 1 Cl.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07084170B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-09dbf5b4d43440c18a10b96ec12ac8d1 |
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| Source note | uspto-grants-2006_08 |
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