tert-Butyl bromoacetate → Tert-butyl (2-bromo-4-trifluoromethylphenoxy)acetate
反応式
[C:1]([O:5][C:6](=[O:17])[CH2:7][O:8][C:9]1[CH:14]=[CH:13][C:12](Cl)=[CH:11][C:10]=1[Br:16])([CH3:4])([CH3:3])[CH3:2].BrC1C=C([C:25]([F:28])([F:27])[F:26])C=CC=1O.BrCC(OC(C)(C)C)=O>>[C:1]([O:5][C:6](=[O:17])[CH2:7][O:8][C:9]1[CH:14]=[CH:13][C:12]([C:25]([F:28])([F:27])[F:26])=[CH:11][C:10]=1[Br:16])([CH3:4])([CH3:3])[CH3:2]参加物
4
実験手順
Following the general method as outlined in Intermediate 1, starting from 2-bromo-4-(trifluoromethyl)phenol and tert-butyl bromoacetate (Aldrich), the title compound was obtained as a dark orange sticky solid in quantitative yield.
出典と根拠
- ORDレコード
- ord-7c743510e981458c86050c046a9f8794
- 出典データセット
- uspto-grants-2012_09
- 特許番号
- US08273769B2
反応ノート
読み込み中…