HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1173645Generated: October 27, 2026
Sodium Bicarbonate → 4-Amino-2-chloro-3-fluorobenzonitrile
https://huagongshe.com/reaction/1173645
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | N-(3-chloro-4-cyano-2-fluorophenyl)acetamide | HCID 67105224 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Amino-2-chloro-3-fluorobenzonitrile | HCID 53416208 | 64% |
Reaction Steps
A mixture of N-(4-bromo-3-chloro-2-fluorophenyl)acetamide (17.0 g) and copper(I) cyanide (5.88 g) in N,N-dimethylformamide was stirred at 150° C. overnight. After warming to room temperature, water was added, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over magnesium sulfate, and the solvent was evaporated under reduced pressure to give N-(3-chloro-4-cyano-2-fluorophenyl)acetamide. Ethanol (250 ml)-concentrated hydrogen chloride (26.6 mL) was added to N-(3-chloro-4-cyano-2-fluorophenyl)acetamide, and the mixture was refluxed overnight. The mixture was ice-cooled, and neutralized with saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by column, and the obtained solid was washed with hexane to give the title compound as a pale-yellow solid (yield: 7.0 g, 64%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07834051B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-c270f94c9e36417ca8e2e29786729cfc |
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| Source note | uspto-grants-2010_11 |
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