HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1586348Generated: November 1, 2026
Hydrochloric Acid → 3-Bromo-2-chloro-5-methylbenzoic acid
https://huagongshe.com/reaction/1586348
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 2-Amino-3-bromo-5-methylbenzoic acid | HCID 2774400 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 3-Bromo-2-chloro-5-methylbenzoic acid | HCID 15839796 | 58% |
Reaction Steps
The diazonium chloride of 2-amino-3-bromo-5-methylbenzoic acid is obtained by running an aqueous sodium nitrite solution (0.013 mol) dropwise at -5° C. onto a solution containing 0.0109 mol of 2-amino-3-bromo-5-methylbenzoic acid, 10 ml of hydrochloric acid, 10 ml of water and 30 ml of acetic acid. The reaction mixture is then stirred at 0° C. for 30 minutes and then poured into a large-volume round-bottomed flask containing 0.013 mol of cuprous chloride in 10 ml of acetic acid. The mixture obtained is brought to 60° C., stirred for 2 hours, and then hydrolysed after cooling by addition of ice. The precipitate obtained is filtered and washed with water. 3-Bromo-2-chloro-5-methylbenzoic acid is obtained: (Yield 58%, M.p. 160° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05945382 |
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| Source dataset | uspto-grants-1999_08 |
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| ORD ID | ord-225756f206a84506a03001a6115dc5fe |
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| Source note | uspto-grants-1999_08 |
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