Sulfuric Acid → Benzoic acid, 5-sulfino-2-(trifluoromethoxy)-

HRID 1820723노트

반응식

HRID 1820723 반응식
Cl[S:2]([C:5]1[CH:6]=[CH:7][C:8]([O:14][C:15]([F:18])([F:17])[F:16])=[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>[S:2]([C:5]1[CH:6]=[CH:7][C:8]([O:14][C:15]([F:16])([F:17])[F:18])=[C:9]([CH:13]=1)[C:10]([OH:12])=[O:11])([OH:4])=[O:3]

참가 물질

6

반응물 4

HCID 1118Sulfuric AcidHCID 14798Sodium HydroxideHCID 24437Sodium SulfiteHCID 866007055-(Chlorosulfonyl)-2-(trifluoromethoxy)benzoic acid2회

생성물 1

HCID 69037717Benzoic acid, 5-sulfino-2-(trifluoromethoxy)-수율 99.2%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

5-chlorosulfonyl-2-trifluoromethoxy-benzoic acid (1.0 g, compound 2.9.a) was added portionwise onto a solution of sodium sulfite (3.1 g) in 16 mL 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. The solution was then extracted several times with diethyl ether and ethyl acetate. The combined organic phases were dried (sodium sulfate) and concentrated in vacuo to yield the title compound as a white solid (0.88 g).

후처리

  1. temperatureAfter such time the reaction mixture was cooled down with an ice bath
  2. extractionThe solution was then extracted several times with diethyl ether and ethyl acetate
  3. dry with materialThe combined organic phases were dried (sodium sulfate)
  4. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-853ace481e8847d4823cc5fb22d16bfb
출처 데이터셋
uspto-grants-2009_10
특허 번호
US07605163B2

반응 노트

불러오는 중…