反応式
[C:1]([C:5]1[CH:10]=[CH:9][C:8]([CH2:11][C:12]([O:14]C)=[O:13])=[CH:7][CH:6]=1)([CH3:4])([CH3:3])[CH3:2].O>CO>[C:1]([C:5]1[CH:10]=[CH:9][C:8]([CH2:11][C:12]([OH:14])=[O:13])=[CH:7][CH:6]=1)([CH3:4])([CH3:2])[CH3:3]参加物
4
実験手順
Methyl 4-t-butylphenylacetate (20 mmol) was dissolved in MeOH (160 mL) and treated with water (40 mL) and LiOH monohydrate (30 mmol). The reaction was allowed to stir at room temperature overnight. Volatiles were removed under reduced pressure, the remaining residue was diluted with water and neutralized to ph 4 with 1 N sulfuric acid. The resulting solids were filtered, washed with water and dried to leave 4-t-butylphenylacetic acid as an off-white solid (3.8 g, 99%).
後処理
- customVolatiles were removed under reduced pressure
- additionthe remaining residue was diluted with water
- filtrationThe resulting solids were filtered
- washwashed with water
- customdried
出典と根拠
- ORDレコード
- ord-af08657aad9e4b77a676d6e70de6dc3d
- 出典データセット
- uspto-grants-2002_03
- 特許番号
- US06358945B1
関連ノート
読み込み中…