Potassium bis(trimethylsilyl)amide → 4-Cyclopropanesulfonyl-1,2-difluoro-benzene

HRID 2374242ノート

反応式

HRID 2374242 の反応式
Cl[CH2:2][CH2:3][CH2:4][S:5]([C:8]1[CH:13]=[CH:12][C:11]([F:14])=[C:10]([F:15])[CH:9]=1)(=[O:7])=[O:6].C[Si]([N-][Si](C)(C)C)(C)C.[K+]>C1COCC1>[CH:4]1([S:5]([C:8]2[CH:13]=[CH:12][C:11]([F:14])=[C:10]([F:15])[CH:9]=2)(=[O:7])=[O:6])[CH2:2][CH2:3]1

参加物

4

実験手順

To mmol 4-(3-chloro-propane-1-sulfonyl)-1,2-difluoro-benzene (300 mg, 1.18 mmol) in 10 ml THF at −78° C. was added dropwise a 0.9 M solution of potassium bis(trimethylsilyl)amide in THF (3.65 ml, 3.32 mmol). The reaction mixture was then allowed to warm to RT and stirring continued for a further 30 min at RT. The mixture was quenched by addition of 1 M aq HCl (2 ml) and water (10 ml), and then extracted three times with ethyl acetate. The combined organic phases were dried with Na2SO4, and concentrated in vacuo. The residue was chromatographed over SiO2 (ethyl acetate/heptane 1:10) to afford the title compound (90 mg, 37%) as an off-white amorphous solid. MS (ISP): 219.2 MH+

後処理

  1. customThe mixture was quenched by addition of 1 M aq HCl (2 ml) and water (10 ml)
  2. extractionextracted three times with ethyl acetate
  3. dry with materialThe combined organic phases were dried with Na2SO4
  4. concentrationconcentrated in vacuo
  5. customThe residue was chromatographed over SiO2 (ethyl acetate/heptane 1:10)

出典と根拠

ORDレコード
ord-1aae440adf3f4e2bb7fb8ea7ce05aeb5
出典データセット
uspto-grants-2008_12
特許番号
US07462617B2

反応ノート

読み込み中…