反応式
Cl[CH2:2][C:3]([OH:5])=[O:4].[CH2:6]([NH:8][CH2:9][CH3:10])[CH3:7]>>[CH2:6]([N:8]([CH2:2][C:3]([OH:5])=[O:4])[CH2:9][CH3:10])[CH3:7]参加物
3
実験手順
A solution of chloroacetic acid (30 g, 0.32 mol) in diethylamine (230 mL, 2.2 mol) was stirred overnight. The obtained white precipitate was removed by filtration. The filtrate was evaporated to dryness to afford yellow oil to which EtOAc (300 mL) was added. The obtained precipitate was again removed by filtration. The filtrate was evaporated to afford yellow solid residue (44 g) that was washed with hexane (2×100 mL), EtOAc (2×50 mL) and again with hexane (50 mL), and then dried in vacuo to afford title Intermediate 2 (38 g).
後処理
- customThe obtained white precipitate was removed by filtration
- customThe filtrate was evaporated to dryness
- customto afford yellow oil to which EtOAc (300 mL)
- additionwas added
- customThe obtained precipitate was again removed by filtration
- customThe filtrate was evaporated
出典と根拠
- ORDレコード
- ord-c050af519d4d4415a82bd6b1297327ed
- 出典データセット
- uspto-grants-2012_07
- 特許番号
- US08227428B2
関連ノート
読み込み中…