반응식
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]참가 물질
5
실험 절차
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°.
후처리
- 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
출처 및 근거
- ORD 기록
- ord-3d84c3f678a24b7e9b92c4cbcf018d63
- 출처 데이터셋
- uspto-grants-1976_08
- 특허 번호
- US03975537
연결된 노트
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