HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 363754Generated: October 25, 2026
Sodium Hydroxide → 6-Amino-3-bromo-2-methylbenzonitrile
https://huagongshe.com/reaction/363754
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-Amino-6-methylbenzonitrile | HCID 279973 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-Amino-3-bromo-2-methylbenzonitrile | HCID 22465737 | 92.5% |
Reaction Steps
A stirred solution of 8.3 grams (0.063 mole) of 2-amino-6-methylbenzonitrile in 125 mL of N,N-dimethylformamide was cooled in an ice bath, and a solution of 11.2 grams (0.063 mole) of N-bromosuccinimide in 125 mL of N,N-dimethylformamide was added dropwise during a 30 minute period, while maintaining the reaction mixture temperature at about 15°-25° C. Upon completion of addition, the reaction mixture was stirred at ambient temperature for about 20 hours. After this time, the reaction mixture was poured into 1 liter of aqueous 3N sodium hydroxide. The mixture was then diluted to a volume of about 1700 mL with distilled water. A solid precipitate was collected by filtration and dried under reduced pressure, yielding 12.3 grams of 2-amino-5-bromo-6-methylbenzonitrile, mp 111°-113° C. The NMR spectrum was consistent with the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05874579 |
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| Source dataset | uspto-grants-1999_02 |
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| ORD ID | ord-2219382b6c6a4f82bba25cea4ba8cb9f |
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| Source note | uspto-grants-1999_02 |
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