反応式
[OH-].[K+].[NH:3]1[CH:7]=[CH:6][CH:5]=[CH:4]1.Br[CH2:9][C:10]([O:12]CC)=[O:11].Cl>O.CS(C)=O>[N:3]1([CH2:9][C:10]([OH:12])=[O:11])[CH:7]=[CH:6][CH:5]=[CH:4]1参加物
7
実験手順
To a mixture of potassium hydroxide (16.7 g) and dry DMSO (150 mL), pyrrole (5 g) was added dropwise at 20-25° C., with stirring under nitrogen atmosphere. Stirring was continued for 1 hr at 20-25° C. Ethyl bromoacetate (24.5 g) was added dropwise at 20-25° C. and stirring was continued for 2 hr. In the reaction mixture (150 mL) DM water was added and pH was made acidic (pH=3) with 20% HCl (50 mL). The reaction mixture was extracted with diethyl ether (2×100 mL). The combined organic extract was washed with DM water (100 mL), saturated brine (100 mL) and dried over Na2SO4. The solvent was evaporated to obtain pyrrol-1-yl-acetic acid.
後処理
- additionwas added dropwise at 20-25° C.
- stirringStirring
- stirringstirring
- waitwas continued for 2 hr
- extractionThe reaction mixture was extracted with diethyl ether (2×100 mL)
- extractionThe combined organic extract
- washwas washed with DM water (100 mL), saturated brine (100 mL)
- dry with materialdried over Na2SO4
- customThe solvent was evaporated
出典と根拠
- ORDレコード
- ord-e2f9c2f5ea444841af1fe7338d03a096
- 出典データセット
- uspto-grants-2012_02
- 特許番号
- US08110598B2
関連ノート
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