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Nitric Acid → 3-Nitro-5-pentafluorosulfanylbenzoic Acid

HRID 249711
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HRID 249711 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]
참가 물질실험 절차후처리출처 및 근거반응 노트

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 (3.0 g) was dissolved in fuming nitric acid (20 ml) and stirred at RT with exclusion of moisture. Concentrated sulfuric acid (1.5 ml) was then added and the mixture was stirred at 75° C. After stirring at 75° C. for 6 h, it was allowed to stand overnight, then further sulfuric acid (1.5 ml) was added and the mixture was heated at 75° C. for 8 h. After allowing to stand overnight, it was added to ice water and stirred for 2 h. The commencing crystallization was completed overnight in a refrigerator. The precipitate was then filtered off with suction and dried in a high vacuum. 2.7 g of 3-pentafluorosulfanyl-5-nitrobenzoic acid were obtained. It was possible to obtain a further 530 mg from the mother liquor after extracting three times with methylene chloride, drying the combined methylene chloride phases over magnesium sulfate and concentrating the solvent.

후처리

  1. stirringthe mixture was stirred at 75° C
  2. stirringAfter stirring at 75° C. for 6 h
  3. temperaturethe mixture was heated at 75° C. for 8 h
  4. waitto stand overnight
  5. stirringstirred for 2 h
  6. customThe commencing crystallization
  7. waitwas completed overnight in a refrigerator
  8. filtrationThe precipitate was then filtered off with suction
  9. customdried in a high vacuum

출처 및 근거

ORD 기록
ord-97bf593556c64ce99f76d3919c31cef7
출처 데이터셋
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07863269B2

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