Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Chlorophenol | HCID 7245 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-Fluoro-2-nitrobenzene | HCID 73895 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 3432930 | HCID 3432930 | — |
Reaction Steps
Sodium hydride (1.00 g) was added in portions to a solution of 2-chlorophenol (5.00 g) in N,N-dimethylformamide (100 mL) under nitrogen. To the resulting solution was added 2-fluoro-1-nitrobenzene (5.00 g). The mixture was heated at 65° C. overnight, and then was evaporated under vacuum. The residue was partitioned between chloroform and 1 N NaOH, and the layers were separated. The aqueous layer was extracted once more with chloroform, and the combined chloroform layers were washed with water and brine, dried over magnesium sulfate, and evaporated under vacuum to a yellow oil. The oil was crystallized from ethyl ether/hexane at -78° C. to yield the title compound as a light yellow solid. Mp: 48°-49° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05304644 |
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| Source dataset | uspto-grants-1994_04 |
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| ORD ID | ord-c7d56218c9d04584ad870404ed4d4f20 |
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| Source note | uspto-grants-1994_04 |
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