HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1042346Generated: October 31, 2026
Dimethylformamide → 3-Chloro-2-fluorophenylacetic acid
https://huagongshe.com/reaction/1042346
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1-(Bromomethyl)-3-chloro-2-fluorobenzene | HCID 522827 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Chloro-2-fluorophenylacetic acid | HCID 2773720 | — |
Reaction Steps
1-Bromomethyl-3-chloro-2-fluoro-benzene (10.00 g, 44.80 mmol) and KCN (5.80 g, 89.07 mmol) were mixed in DMF and the resulting reaction mixture was stirred at 75° C. for 2 days. The reaction mixture was cooled to room temperature, and water was added. The mixture was extracted with Et2O (3×300 mL). The combined organic phases were washed with H2O (2×200 mL) and brine (1×200 mL), then dried over MgSO4 and concentrated. The crude nitrile was taken up in water and KOH (5.00 g, 89.11 mmol) was added. The resulting mixture was refluxed for 14 hours. After cooling to room temperature, the reaction mixture was diluted with water and washed with Et2O (2×150 mL). The aqueous layer was acidified with concentrated HCl and was extracted with Et2O (3×300 mL). The combined organic phases were washed with H2O (2×200 mL) and brine (1×200 mL), then dried over MgSO4 and concentrated to afford the title acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08557853B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-456c73bedac24f66a62015c9fe44fc2a |
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| Source note | uspto-grants-2013_10 |
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