Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | N-[7-(Trifluoromethyl)-2-naphthalenyl]acetamide | HCID 18451538 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 18451486 | HCID 18451486 | — |
Reaction Steps
A mixture of 7-trifluoromethyl-2-acetamidonaphthalene (620 mg, 2.45 mmol), N-chlorosuccinimide (326 mg, 2.45 mmol) and 1 M HCl in acetic acid (2.45 mL, 2.45 mmol) in acetic acid (10 mL) is heated at 50° C. under a N2 atmosphere for 1 hour. After cooling to room temperature, the mixture is partitioned between EtOAc and water. The organic layer is washed with brine, dried (Na2SO4) and concentrated by rotary evaporator to give 1-chloro-7-trifluoromethyl-2-acetamidonaphthalene as an off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07202364B2 |
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| Source dataset | uspto-grants-2007_04 |
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| ORD ID | ord-34f63787d3f44d69bbf028e79cf80b27 |
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| Source note | uspto-grants-2007_04 |
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