Sulfuric Acid → 2-Fluoro-5-sulfinobenzoic acid

HRID 225721ノート

反応式

HRID 225721 の反応式
Cl[S:2]([C:5]1[CH:6]=[CH:7][C:8]([F:14])=[C:9]([CH:13]=1)[C:10]([OH:12])=[O:11])(=[O:4])=[O:3].S([O-])([O-])=O.[Na+].[Na+].[OH-].[Na+].OS(O)(=O)=O>O>[F:14][C:8]1[CH:7]=[CH:6][C:5]([S:2]([OH:4])=[O:3])=[CH:13][C:9]=1[C:10]([OH:12])=[O:11]

参加物

6

反応物 4

HCID 1118Sulfuric AcidHCID 14798Sodium HydroxideHCID 24437Sodium SulfiteHCID 6089842-Fluoro-5-chlorosulfonylbenzoic acid

生成物 1

HCID 577535332-Fluoro-5-sulfinobenzoic acid収率 72%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

264 mmol 5-Chlorosulfonyl-2-fluoro-benzoic acid (CAS: 37098-75-2) was added portionwise onto a solution of 1.98 mol sodium sulfite in 1 L of water. The reaction mixture was kept under basic conditions by the addition of the proper amount of 20% NaOH and was stirred at room temperature for 45 minutes. After such time the reaction mixture was cooled down with an ice bath and was then acidified by the addition of 20% H2SO4 solution until reaching pH 2. Water was evaporated and 600 ml methanol was added. The mixture was stirred overnight and filtrated. The filtrate was evaporated and dried to yield the title compound as a white solid (72%). MS (m/e): 203.0 ([M−H, 100%)

後処理

  1. temperatureAfter such time the reaction mixture was cooled down with an ice bath
  2. customWater was evaporated
  3. addition600 ml methanol was added
  4. stirringThe mixture was stirred overnight
  5. filtrationfiltrated
  6. customThe filtrate was evaporated
  7. customdried

出典と根拠

ORDレコード
ord-3c32b952a9b6479e9f4215f898b59b86
出典データセット
uspto-grants-2009_07
特許番号
US07557114B2

反応ノート

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