反応式
[CH2:1]([CH2:3][NH2:4])[OH:2].[SH2]=N.[C:7]1([NH:13][C:14](C2C=CC=CC=2C(O)=O)=[O:15])[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1>CC(C)=O>[C:7]1([NH:13][C:14]([NH:4][CH2:3][CH2:1][OH:2])=[O:15])[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1参加物
4
実験手順
A solution of 0.65 g ethanolamine with 5 ml aceton was added dropwise to a suspension of 1.5 g phenylcarbamoyl-benzoic acid sulfimide with 10 ml aceton, under stirring. The reaction mixture was stirred for a further 30 minutes at ambient temperature, evaporated in vacuo, the residue was triturated with 20 ml water, and the obtained solid product was filtered, dried and recrystallized. There was obtained 0.25 g 1-phenyl-3-(2-hydroxyethyl)-urea, melting at 120°-122° C.
後処理
- stirringThe reaction mixture was stirred for a further 30 minutes at ambient temperature
- customevaporated in vacuo
- customthe residue was triturated with 20 ml water
- filtrationthe obtained solid product was filtered
- customdried
- customrecrystallized
出典と根拠
- ORDレコード
- ord-6a4bc0185b8a4f68ba06f1ee91d1b5f7
- 出典データセット
- uspto-grants-1984_03
- 特許番号
- US04435567
関連ノート
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