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Hydrochloric Acid → 2-Chloro-4-fluoro-5-aminophenyl methanesulfonate

HRID 580274
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HRID 580274 반응식
[CH3:1][S:2]([O:5][C:6]1[CH:11]=[C:10]([N+:12]([O-])=O)[C:9]([F:15])=[CH:8][C:7]=1[Cl:16])(=[O:4])=[O:3].Cl.[OH-].[Na+]>O.[Fe]>[CH3:1][S:2]([O:5][C:6]1[CH:11]=[C:10]([NH2:12])[C:9]([F:15])=[CH:8][C:7]=1[Cl:16])(=[O:3])=[O:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 137982292-Chloro-4-fluoro-5-nitrophenyl methanesulfonate

생성물 1

HCID 137982302-Chloro-4-fluoro-5-aminophenyl methanesulfonate수율 92.9%

시약·촉매·용매 2

HCID 23925Iron촉매HCID 962Water
용매

실험 절차

A suspension of 2-chloro-4-fluoro-5-nitrophenyl methanesulfonate (27.0 g) and iron (33.5 g) in water (140 ml) was heated for reduction of the nitro group into amino group. When the temperature of the reaction mixture reached 80° C., 35% hydrochloric acid (3.2 g) was added thereto. Upon cooling to room temperature, the pH of the reaction mixture was adjusted to 9.0 with the addition of an aqueous sodium hydroxide solution. The reaction mixture was then extracted with toluene and tetrahydrofuran. The organic layer so separated was washed with water, dried over anhydrous sodium sulfate and then distilled under reduced pressure to remove the solvent, affording the titled compound (22.3 g) as a pale yellow oil which was then purified by silica gel chromatography to give colorless crystals with melting point 79°-80° C.

후처리

  1. temperaturewas heated for reduction of the nitro group into amino group
  2. customreached 80° C.
  3. extractionThe reaction mixture was then extracted with toluene and tetrahydrofuran
  4. customThe organic layer so separated
  5. washwas washed with water
  6. dry with materialdried over anhydrous sodium sulfate
  7. distillationdistilled under reduced pressure
  8. customto remove the solvent

출처 및 근거

ORD 기록
ord-fe01b259de49419b95da5a3a723218c8
출처 데이터셋
uspto-grants-1988_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04752326

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