HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522471Generated: October 30, 2026
Water → 5-Amino-2-fluoro-4-methylbenzonitrile
https://huagongshe.com/reaction/522471
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 5-Bromo-4-fluoro-2-methylaniline | HCID 2782786 | — |
| Reactant | HCID 178418546 | HCID 178418546 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 5-Amino-2-fluoro-4-methylbenzonitrile | HCID 86677449 | 68.5% |
Reaction Steps
The starting 5-bromo-4-fluoro-2-methylaniline (1) (20 g, 98 mmol) was dissolved in anhydrous 1-methylpyrrolidinone (100 mL), and copper (I) cyanide (17.6 g, 196 mmol) was added. The reaction was heated to 180° C. for 3 hours, cooled to room temperature, and water (300 mL) and concentrated ammonium hydroxide (300 mL) added. The mixture was stirred for 30 minutes and extracted with EA (3×200 mL). The combined extracts were dried over magnesium sulfate, and the solvent was removed under reduced pressure. The oily residue was washed with hexanes (2×100 mL), and the solid dissolved in dichloromethane and loaded onto a silica gel column. Eluting with 0 to 25% EA in hexanes gradient provided 5-amino-2-fluoro-4-methylbenzonitrile (10.06 g, 67.1 mmol). LC/MS (m/z: 151 M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09333197B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-16fad01f38664e5b935cab11bf5e7d97 |
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| Source note | uspto-grants-2016_05 |
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