HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1663409Generated: October 28, 2026
Acetonitrile → 3-(4-Chloro-2-fluorophenyl)-3-oxopropanenitrile
https://huagongshe.com/reaction/1663409
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | 4-Chloro-2-fluorobenzoate | HCID 6931880 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 3-(4-Chloro-2-fluorophenyl)-3-oxopropanenitrile | HCID 24706670 | 97.4% |
Reaction Steps
A 1.6 M hexane solution of n-butyllithium (39.8 mL, 63.6 mmol) was added to a solution of diisopropylamine (9.45 mL, 66.3 mmol) in THF (100 mL) at −78° C. over 10 min. The resultant solution was stirred at 0° C. for 30 min and cooled to −78° C. Acetonitrile (3.32 mL, 63.6 mmol) dropwise. The mixture was stirred at −78° C. for 30 min and then added a solution of 4-chloro-2-fluorobenzoate (5.00 g, 26.5 mmol) in THF (5 mL) at −78° C. dropwise. After stirring for 1 h at −78° C., the reaction mixture was quenched with brine (20 mL), warmed to room temperature and adjusted to pH 1-2 with 1N aqueous HCl. Following addition of ethyl acetate (400 mL), the mixture was washed with water (40 mL), brine (40 mL), dried (MgSO4) and concentrated to provide 3-(4-chloro-2-fluorophenyl)-3-oxopropanenitrile as tan solid (5.10 g, 97%). MS (ES+) m/z: 198 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08034940B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-28419f3597464cb7b8b27c0509d7d643 |
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| Source note | uspto-grants-2011_10 |
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