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Sodium hydride → 7-fluoro-2-methyl-3,4-dihydro-2H-5,1,2-benzoxathiazepine 1,1-dioxide

HRID 548746
ノート
印刷プレビュー

反応式

HRID 548746 の反応式
[H-].[Na+].F[C:4]1[CH:9]=[C:8]([F:10])[CH:7]=[CH:6][C:5]=1[S:11]([N:14]([CH2:16][CH2:17][OH:18])[CH3:15])(=[O:13])=[O:12]>CN(C=O)C>[F:10][C:8]1[CH:9]=[CH:4][C:5]2[S:11](=[O:13])(=[O:12])[N:14]([CH3:15])[CH2:16][CH2:17][O:18][C:6]=2[CH:7]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 24758Sodium hydrideHCID 576631632,4-difluoro-N-(2-hydroxyethyl)-N-methylbenzenesulfonamide

生成物 1

HCID 576631787-fluoro-2-methyl-3,4-dihydro-2H-5,1,2-benzoxathiazepine 1,1-dioxide収率 58.7%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

Sodium hydride (60% dispersion in mineral oil) (700 mg, 17.51 mmol) was added to a solution of 2,4-difluoro-N-(2-hydroxyethyl)-N-methylbenzenesulfonamide (2 g, 7.96 mmol) in DMF (200 mL) and the mixture stirred at RT for 48 hours. The solvent removed in vacuo, iced water (200 mL) added and the mixture extracted into ethyl acetate. The combined organic extract was washed with brine (40 mL), dried (MgSO4), filtered and reduced in vacuo to give a white solid which was chromatographed on silica, eluting with 20-50% ethyl acetate in isohexane, to give the desired compound as a white solid (1.08 g).

後処理

  1. customThe solvent removed in vacuo, iced water (200 mL)
  2. additionadded
  3. extractionthe mixture extracted into ethyl acetate
  4. extractionThe combined organic extract
  5. washwas washed with brine (40 mL)
  6. dry with materialdried (MgSO4)
  7. filtrationfiltered
  8. customto give a white solid which
  9. customwas chromatographed on silica
  10. washeluting with 20-50% ethyl acetate in isohexane

出典と根拠

ORDレコード
ord-a4c1aa5ecf144371b19fe76a49ec5985
出典データセット
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07943607B2

反応ノート

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