Carbon tetrabromide → Methanesulfonic acid 2-bromomethyl-5-methylphenyl ester
反応式
O[CH2:2][C:3]1[CH:8]=[CH:7][C:6]([CH3:9])=[CH:5][C:4]=1[O:10][S:11]([CH3:14])(=[O:13])=[O:12].C(Br)(Br)(Br)[Br:16].C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>C(Cl)Cl>[Br:16][CH2:2][C:3]1[CH:8]=[CH:7][C:6]([CH3:9])=[CH:5][C:4]=1[O:10][S:11]([CH3:14])(=[O:13])=[O:12]参加物
5
実験手順
To a solution of methanesulfonic acid 2-hydroxymethyl-5-methylphenyl ester (864 mg, 4 mmol) in DCM (45 mL) is added CBr4 (2.0 g, 6 mmol) and PPh3 (1.57 g, 6 mmol). The mixture is stirred at RT for 6 h. The solvent is removed and the residue is purified to give the title compound as a solid.
後処理
- customThe solvent is removed
- customthe residue is purified
出典と根拠
- ORDレコード
- ord-65b1e38750a7478f928d025ca4b99136
- 出典データセット
- uspto-grants-2012_08
- 特許番号
- US08252820B2
反応ノート
読み込み中…