反応式
[Br:1][C:2]1[C:3]([O:13][CH3:14])=[C:4]([C:8]([O:11][CH3:12])=[CH:9][CH:10]=1)[C:5]([OH:7])=[O:6].S(Cl)(Cl)=O.CO.[CH2:21](N(CC)CC)C>C(Cl)Cl>[Br:1][C:2]1[C:3]([O:13][CH3:14])=[C:4]([C:8]([O:11][CH3:12])=[CH:9][CH:10]=1)[C:5]([O:7][CH3:21])=[O:6]参加物
6
実験手順
3-Bromo-2,6-dimethoxybenzoic acid (5.0 g, 19.2 mmol) and thionyl chloride (10 ml) were heated to reflux for 2 h. The mixture was then concentrated in vacuo and diluted with CH2Cl2 (20 ml) and added to a solution of MeOH (614 mg, 38.4 mmol) and triethylamine (3.88 g, 38.4 mmol) in CH2Cl2 (100 ml) at 0° C. The resulting mixture was allowed to warm to RT and stirred for 64 h. The organics were washed with 10% HCl (50 ml), brine (50 ml) and dried (MgSO4) and purified by chromatography (0–50% EtOAC in heptane) to leave a white solid (4.17 g).
後処理
- temperatureto reflux for 2 h
- concentrationThe mixture was then concentrated in vacuo
- additiondiluted with CH2Cl2 (20 ml)
- washThe organics were washed with 10% HCl (50 ml), brine (50 ml)
- dry with materialdried (MgSO4)
- custompurified by chromatography (0–50% EtOAC in heptane)
出典と根拠
- ORDレコード
- ord-6457be78d84249448fa0ee2b08f904df
- 出典データセット
- uspto-grants-2006_11
- 特許番号
- US07138527B2
関連ノート
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