Pyridine → HCID 15067105、化合物
反応式
[CH2:1]([O:3][CH2:4][CH2:5][OH:6])[CH3:2].N1C=CC=CC=1.[S:13](Cl)([CH3:16])(=[O:15])=[O:14]>O1CCCC1>[CH3:16][S:13]([O:6][CH2:5][CH2:4][O:3][CH2:1][CH3:2])(=[O:15])=[O:14]参加物
5
実験手順
To 30g of 2-ethoxyethanol in 300ml of tetrahydrofuran 27.4ml of pyridine were added and 26.4ml of mesyl chloride added dropwise at room temperature over 15 minutes. The mixture was refluxed overnight, the solid that formed filtered off and the solvent evaporated off from the residue. The residue was distilled under 20m Hg to give 2-ethoxyethyl methanesulphonate.
後処理
- temperatureThe mixture was refluxed overnight
- customthe solid that formed
- filtrationfiltered off
- customthe solvent evaporated off from the residue
- distillationThe residue was distilled under 20m Hg
出典と根拠
- ORDレコード
- ord-f8da1dc8ee6d42478c217b4800fba461
- 出典データセット
- uspto-grants-1991_12
- 特許番号
- US05071468
反応ノート
読み込み中…