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Nitric Acid → 3-Nitro-5-pentafluorosulfanylbenzoic Acid

HRID 217762
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HRID 217762 반응식
[F:1][S:2]([F:15])([F:14])([F:13])([F:12])[C:3]1[CH:4]=[C:5]([CH:9]=[CH:10][CH:11]=1)[C:6]([OH:8])=[O:7].S(=O)(=O)(O)O.[N+:21]([O-])([OH:23])=[O:22]>>[F:1][S:2]([F:12])([F:13])([F:14])([F:15])[C:3]1[CH:4]=[C:5]([CH:9]=[C:10]([N+:21]([O-:23])=[O:22])[CH:11]=1)[C:6]([OH:8])=[O:7]
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참가 물질

4

반응물 3

HCID 944Nitric AcidHCID 1118Sulfuric Acid2회HCID 27792093-(Pentafluorosulfanyl)benzoic acid

생성물 1

HCID 596421523-Nitro-5-pentafluorosulfanylbenzoic Acid

실험 절차

3-Pentafluorosulfanylbenzoic acid (5.0 g) was dissolved in fuming nitric acid (20 ml) and stirred at RT with exclusion of moisture. Then concentrated sulfuric acid (3 ml) was added and the mixture was stirred at 75° C. After stirring at 75° C. for 5 h, further sulfuric acid (1.5 ml) was added and, after stirring at 75° C. for 2 h, left to stand overnight. Then the mixture was added to ice-water and stirred for 2 h. The precipitate formed was filtered off with suction and dried under high vacuum. 4.2 g of 3-pentafluorosulfanyl-5-nitrobenzoic acid were obtained. A further 900 mg were obtained from the mother liquor after extracting three times with methylene chloride, drying the combined methylene chloride phases over magnesium sulfate and concentrating the solvent. The precipitate was used in the next stage without further purification.

후처리

  1. stirringthe mixture was stirred at 75° C
  2. stirringAfter stirring at 75° C. for 5 h
  3. stirringafter stirring at 75° C. for 2 h
  4. waitleft
  5. stirringstirred for 2 h
  6. customThe precipitate formed
  7. filtrationwas filtered off with suction
  8. customdried under high vacuum

출처 및 근거

ORD 기록
ord-6b58f33f4bf04d15be1b5893f82d181f
출처 데이터셋
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08198272B2

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