Propionyl chloride → 3-(N-propionyl-N-n-propylamino)chroman
反応式
[C:1](Cl)(=[O:4])[CH2:2][CH3:3].[CH2:6]([NH:9][CH:10]1[CH2:19][C:18]2[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=2)[O:12][CH2:11]1)[CH2:7][CH3:8]>C(Cl)Cl.[OH-].[Na+]>[C:1]([N:9]([CH:10]1[CH2:19][C:18]2[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=2)[O:12][CH2:11]1)[CH2:6][CH2:7][CH3:8])(=[O:4])[CH2:2][CH3:3]参加物
5
実験手順
Propionyl chloride (2.8 g, 29 mmol) was added to a mixture of 15 (1.2 g, 6.4 mmol) in CH2Cl2 and 5% aqueous NaOH. The mixture was stirred for 30 min and separated. The organic layer was extracted with water, separated and dried (MgSO4). The crude product was chromatographed (SiO2) with light petroleum-ether (2:1) as eluant yielding 0.98 g (62%) of 3-(N-propionyl-N-n-propylamino)chroman (16).
後処理
- customseparated
- extractionThe organic layer was extracted with water
- customseparated
- dry with materialdried (MgSO4)
- customThe crude product was chromatographed (SiO2) with light petroleum-ether (2:1) as eluant
出典と根拠
- ORDレコード
- ord-102627aca7b4441bac4d72d68df5c88a
- 出典データセット
- uspto-grants-1994_02
- 特許番号
- US05288748
反応ノート
読み込み中…