1-Bromo-3-methylbutane → Thiophene, 2-isopentyl-

HRID 235093

反応式

HRID 235093 の反応式
[CH2:1](Br)[CH2:2][CH:3]([CH3:5])[CH3:4].[Li][C:8]1[S:9][CH:10]=[CH:11][CH:12]=1>O>[CH3:4][CH:3]([CH3:5])[CH2:2][CH2:1][C:8]1[S:9][CH:10]=[CH:11][CH:12]=1

参加物

4

反応条件

温度
0 °C

実験手順

Isopentyl bromide (Aldrich, 8 g, 53mmol) was added to 53 mL of an ice-cooled solution of lithiothiophene (1.0M in THF, 53 mmol). The reaction was stirred at 0° C. for 2 hours, at room temperature for 16 hours, and poured into water, then the mixture was extracted with hexane. The organic layer was dried and concentrated, and the residue was purified by column chromatography on silica gel, eluting with hexane, to give 7.2 g (88% yield) of the title compound as a colorless oil. NMR (CDCl3) δ:7.10 (dd, J=1, 6 Hz, 1H), 6.90 (dd, J=4, 6 Hz, 1H), 6.78 (dd, J=1, 4 Hz, 1H), 2.84 (t, J=8 Hz, 2H), 1.7-1.5 (m, 3H), 0.94 (d, J=6 Hz, 6H).

後処理

  1. extractionthe mixture was extracted with hexane
  2. customThe organic layer was dried
  3. concentrationconcentrated
  4. customthe residue was purified by column chromatography on silica gel
  5. washeluting with hexane

出典と根拠

ORDレコード
ord-524b9e03480a4f4b83c07433c4943f12
出典データセット
uspto-grants-1997_01
特許番号
US05597832

関連ノート

読み込み中…