反応 #712872

ord-66313e4cd27a45ae9684abc7670069b3

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    洗浄then washed with 1 M aqueous hydrochloric acid
  2. 2
    その他dried
  3. 3
    その他the solvent removed under vacuum
  4. 4
    その他The residue is purified by flash chromatography (0-30% ethyl acetate in cyclohexane)

実験手順

3-Methyl-1,3-butanediol (1.5 mL, 14.1 mmol) is suspended in dry dichloromethane (5 mL) and pyridine (1.24 mL, 15.46 mmol) is added followed by 4-toluenesulfonyl chloride (2.68 g, 14.1 mmol). The mixture is stirred overnight then washed with 1 M aqueous hydrochloric acid, dried and the solvent removed under vacuum. The residue is purified by flash chromatography (0-30% ethyl acetate in cyclohexane) to give the title compound. (Yield 970 mg). LC (METHOD 2): tR=5.67 min; Mass spectrum (ES+): m/z=258 [M+H]+.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US09308194B2uspto-grants-2016_04