Water → 6-Bromo-2,3-dihydro-1lambda6-benzothiophene-1,1,3-trione

HRID 1406284ノート

反応式

HRID 1406284 の反応式
[Br:1][C:2]1[CH:11]=[CH:10][C:5]([C:6]([O:8]C)=O)=[C:4]([S:12]([CH3:15])(=[O:14])=[O:13])[CH:3]=1.[H-].[Na+].O>C1COCC1>[Br:1][C:2]1[CH:11]=[CH:10][C:5]2[C:6](=[O:8])[CH2:15][S:12](=[O:14])(=[O:13])[C:4]=2[CH:3]=1

参加物

5

反応物 3

HCID 962WaterHCID 24758Sodium hydrideHCID 53393139Methyl 4-bromo-2-(methylsulfonyl)benzoate

生成物 1

HCID 565941086-Bromo-2,3-dihydro-1lambda6-benzothiophene-1,1,3-trione収率 100%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

To a solution of methyl 4-bromo-2-(methylsulfonyl)benzoate (774 mg, 2.64 mmol) in anhydrous THF (10 mL) was added NaH (60% in mineral, 111 mg, 2.77 mmol). The mixture was stirred at room temperature for 5 hr. The reaction was monitored by LCMS for completion. H2O (1 mL) was added to quench the reaction followed by the addition of aqueous hydrochloric acid (1N, 50 mL) and EtOAc (50 mL). The organic layer was separated, and the water layer was extracted with 2×EtOAc. The combined organic layers were washed with brine, dried over sodium sulfate, filtered, and concentrated to give the title compound (689 mg, 100%) as a white solid.

後処理

  1. customto quench the reaction
  2. additionfollowed by the addition of aqueous hydrochloric acid (1N, 50 mL) and EtOAc (50 mL)
  3. customThe organic layer was separated
  4. extractionthe water layer was extracted with 2×EtOAc
  5. washThe combined organic layers were washed with brine
  6. dry with materialdried over sodium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated

出典と根拠

ORDレコード
ord-42100e23bf474aedb73893928793a97c
出典データセット
uspto-grants-2014_12
特許番号
US08916593B2

反応ノート

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