反応式
C[O:2][C:3](=O)[C:4]1[CH:9]=[CH:8][C:7]([O:10][CH3:11])=[C:6]([Cl:12])[CH:5]=1.[OH-].[Na+].[ClH:16]>O>[Cl:12][C:6]1[CH:5]=[C:4]([CH:9]=[CH:8][C:7]=1[O:10][CH3:11])[C:3]([Cl:16])=[O:2]参加物
5
実験手順
A mixture of 10.4 g. (0.052 mol.) of 3-chloro-4-methoxybenzoic acid methyl ester and 3.5 g. (0.09 mol.) of sodium hydroxide in 150 ml. of water was refluxed for two hours. The reaction mixture was cooled and acidified with 10% aqueous hydrochloric acid to precipitate 3-chloro-4-methoxybenzoic acid, m.p. 199°-202°. The acid was refluxed with thionyl chloride as described in the procedure of Example 9 to give 3-chloro-4-methoxybenzoic acid chloride, m.p. 55°-57°.
後処理
- additionA mixture of 10.4 g
- temperatureThe reaction mixture was cooled
- customto precipitate 3-chloro-4-methoxybenzoic acid, m.p. 199°-202°
- temperatureThe acid was refluxed with thionyl chloride
出典と根拠
- ORDレコード
- ord-3d84c3f678a24b7e9b92c4cbcf018d63
- 出典データセット
- uspto-grants-1976_08
- 特許番号
- US03975537
関連ノート
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