Thionyl Chloride → 3-Benzoyloxy-4-methoxybenzoylchloride
反応式
[C:1]([O:9][C:10]1[CH:11]=[C:12]([CH:16]=[CH:17][C:18]=1[O:19][CH3:20])[C:13](O)=[O:14])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.S(Cl)([Cl:23])=O>C1(C)C=CC=CC=1>[C:1]([O:9][C:10]1[CH:11]=[C:12]([CH:16]=[CH:17][C:18]=1[O:19][CH3:20])[C:13]([Cl:23])=[O:14])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1参加物
4
実験手順
A solution of 3-benzoyloxy-4-methoxybenzoic acid (29.3 g; that is prepared as described in Reference Example 9) in toluene (300 mL) is treated with thionyl chloride (30 mL) and heated on the steam bath for 6 hours. It is then cooled, filtered and concentrated, to give 3-benzoyloxy-4-methoxybenzoyl chloride (28.7 g), m.p. 120-122° C.
後処理
- customthat is prepared
- temperatureheated on the steam bath for 6 hours
- temperatureIt is then cooled
- filtrationfiltered
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-6b6634ac129341dc883ad48766a21053
- 出典データセット
- uspto-grants-2001_07
- 特許番号
- US06255326B1
反応ノート
読み込み中…