Hydrochloric Acid → 3-Chloro-2-methoxybenzoic acid
反応式
N([O-])=O.[Na+].N[C:6]1[C:7]([O:16][CH3:17])=[C:8]([CH:13]=[CH:14][CH:15]=1)[C:9]([O:11]C)=[O:10].[ClH:18]>O.CO.[OH-].[Na+]>[Cl:18][C:6]1[C:7]([O:16][CH3:17])=[C:8]([CH:13]=[CH:14][CH:15]=1)[C:9]([OH:11])=[O:10]参加物
実験手順
A solution of 1.2 g of sodium nitrite in 3 mL of water was added dropwise to a solution of 2 g (0.011 mole) of methyl 3-amino-2-methoxybenzoate in 15 mL of conc. HCl kept below 10° C. After completing the addition, stirring was continued for 0.5 hour at 0° C. The cold solution was then added dropwise to a solution of 2.5 g of cuprous chloride in 6 mL of concentrated HCl at 80°-85° C. After stirring at this temperature for 0.5 hour, the solution was chilled to precipitate an oil which was taken up in methylene chloride. After drying and removing the solvent, the oil obtained above was dissolved in 75 mL of methanol containing 7 mL of 10% NaOH. The solution was heated under reflux for 0.5 hour. After evaporation, the oil was treated with 40 mL of dilute HCl. A white solid precipitated to give 0.5 g (24%) of 3-chloro-2-methoxybenzoic acid after crystallization from ethyl acetate-hexane.
後処理
- customkept below 10° C
- additionthe addition
- stirringAfter stirring at this temperature for 0.5 hour
- temperaturethe solution was chilled
- customto precipitate an oil which
- customAfter drying
- customremoving the solvent
- customthe oil obtained
- temperatureThe solution was heated
- temperatureunder reflux for 0.5 hour
- customAfter evaporation
- additionthe oil was treated with 40 mL of dilute HCl
- customA white solid precipitated
出典と根拠
- ORDレコード
- ord-26c27780e9e64583a5f823fec5d4c225
- 出典データセット
- uspto-grants-1984_09
- 特許番号
- US04470977
反応ノート
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