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3-Nitro-5-pentafluorosulfanylbenzoic Acid → 3-Amino-5-pentafluorosulfanylbenzoic acid

HRID 217758
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인쇄 미리보기

반응식

HRID 217758 반응식
[F:1][S:2]([F:18])([F:17])([F:16])([F:15])[C:3]1[CH:4]=[C:5]([CH:9]=[C:10]([N+:12]([O-])=O)[CH:11]=1)[C:6]([OH:8])=[O:7].[H][H]>CO.[Ni]>[NH2:12][C:10]1[CH:9]=[C:5]([CH:4]=[C:3]([S:2]([F:18])([F:1])([F:15])([F:16])[F:17])[CH:11]=1)[C:6]([OH:8])=[O:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 596421523-Nitro-5-pentafluorosulfanylbenzoic AcidHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 580857063-Amino-5-pentafluorosulfanylbenzoic acid수율 86.9%

시약·촉매·용매 2

HCID 935Nickel촉매HCID 887Methanol용매

실험 절차

Subsequently, the 3-pentafluorosulfanyl-5-nitrobenzoic acid (5 g) was dissolved in methanol (300 ml), Raney nickel (about 750 mg) was added and hydrogenation was effected under a hydrogen atmosphere (hydrogen balloon). After 3 h, the catalyst was filtered off and the filter residue was washed thoroughly with methanol. The filtrate was concentrated and dried. The residue was purified using silica gel (2×50 g cartridge, n-heptane/EA gradient of 0-100% within 60 min). 3.9 g of the title compound were obtained.

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후처리

  1. filtrationthe catalyst was filtered off
  2. washthe filter residue was washed thoroughly with methanol
  3. concentrationThe filtrate was concentrated
  4. customdried
  5. customThe residue was purified
  6. customsilica gel (2×50 g cartridge, n-heptane/EA gradient of 0-100% within 60 min)

출처 및 근거

ORD 기록
ord-ee0c30554f804d4d80a3598974f0622d
출처 데이터셋
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08198272B2

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