HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 1-Chloro-6-fluoro-2-aminonaphthalene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | N-(1-chloro-6-fluoro-2-naphthyl)carbamic acid ethyl ester | HCID 68805760 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-Chloro-6-fluoro-2-aminonaphthalene | HCID 18451483 | — |
Reaction Steps
A mixture of N-(1-chloro-6-fluoro-2-naphthyl)carbamic acid ethyl ester (600 mg, 2.24 mmol) and KOH (1.51 g, 26.9 mmol) in ethanol (20 mL) is heated to reflux temperature under N2 atmosphere for 12 hours. After cooling, the reaction mixture is concentrated by rotary evaporator. The residual oil is purified by flash chromatography on silica gel (3:1 hexanes/EtOAc) to give 1-chloro-6-fluoro-2-aminonaphthalene as a brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07202364B2 |
| Source dataset | uspto-grants-2007_04 |
| ORD ID | ord-99f366b8e9874aa299d46b023460aedf |
| Source note | uspto-grants-2007_04 |