反応式
[NH2:1][C:2]1[CH:3]=[C:4]([CH2:8][C:9]([OH:11])=[O:10])[CH:5]=[CH:6][CH:7]=1.[Cl:12][Si](C)(C)[CH3:14]>CO>[ClH:12].[NH2:1][C:2]1[CH:3]=[C:4]([CH2:8][C:9]([O:11][CH3:14])=[O:10])[CH:5]=[CH:6][CH:7]=1参加物
4
反応条件
- 温度
- 20 °C
実験手順
3-Aminophenylacetic acid (1 wt) was suspended in methanol (5 vol) under nitrogen at 20° C. Chlorotrimethylsilane (1.26 vol) was added over 60 minutes at 20° C. The reaction mixture was stirred at 20° C. for one hour, then concentrated under reduced pressure to 3 vol. Methyl-t-butyl ether (4 vol) was added and the resulting suspension was stirred at room temperature for 18 hours. The solid was collected by filtration, washing with methyl-t-butyl ether (4×1 vol). The material was dried in oven at 40° C. for 5 hours to give the title compound.
後処理
- concentrationconcentrated under reduced pressure to 3 vol. Methyl-t-butyl ether (4 vol)
- additionwas added
- stirringthe resulting suspension was stirred at room temperature for 18 hours
- filtrationThe solid was collected by filtration
- washwashing with methyl-t-butyl ether (4×1 vol)
- customThe material was dried in oven at 40° C. for 5 hours
出典と根拠
- ORDレコード
- ord-4e29d29479dd4036a2642dc99786f17a
- 出典データセット
- uspto-grants-2010_06
- 特許番号
- US07732600B2
関連ノート
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