Sodium Carbonate → HCID 57468838、化合物

HRID 1927983ノート

反応式

HRID 1927983 の反応式
Cl.[CH3:2][O:3][NH2:4].C([O-])([O-])=O.[Na+].[Na+].[Br:11][C:12]1[CH:13]=[C:14]([S:18](Cl)(=[O:20])=[O:19])[CH:15]=[CH:16][CH:17]=1.[OH-].[Na+]>C1COCC1.O.O1CCOCC1>[Br:11][C:12]1[CH:13]=[C:14]([S:18]([NH:4][O:3][CH3:2])(=[O:20])=[O:19])[CH:15]=[CH:16][CH:17]=1

参加物

8

反応条件

温度
23 °C

実験手順

To a solution of commercially available methoxyamine hydrochloride (1.96 g, 23.4 mmol) and 2 M Na2CO3-solution (20 mL, 40 mmol) in THF (100 mL) at 0° C. was added dropwise added commercially available 3-bromobenzenesulfonyl chloride (2.5 g, 9.8 mmol) and the mixture was stirred at 23° C. for 18 h. The reaction is diluted with water, extracted with EtOAc, washed with brine, dried over Na2SO4, filtered and concentrated to give a light brown solid, which was refluxed with 1 M NaOH (10 mL) in dioxane (10 mL) for 30 min to cleave disulfonylated product. Cooled to rt, diluted with water, extracted with EtOAc, washed organic layer with brine and dried over Na2SO4. Removal of the solvent in vacuum left a light brown solid, which was purified by trituration with heptane/diethyl ether gave the title compound as a light yellow solid (1.30 g, 50%). MS (ISN) 264.0 [(M−H)−] and 266.0 [(M+2−H)−].

後処理

  1. extractionextracted with EtOAc
  2. washwashed with brine
  3. dry with materialdried over Na2SO4
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customto give a light brown solid, which
  7. temperatureCooled to rt
  8. extractionextracted with EtOAc
  9. washwashed organic layer with brine
  10. dry with materialdried over Na2SO4
  11. customRemoval of the solvent in vacuum
  12. waitleft a light brown solid, which
  13. customwas purified by trituration with heptane/diethyl ether

出典と根拠

ORDレコード
ord-622d4a2b555a4e2c88904dd6307b187d
出典データセット
uspto-grants-2012_05
特許番号
US08183262B2

反応ノート

読み込み中…