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

HRID 217758
ノート
印刷プレビュー

反応式

HRID 217758 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 596421523-Nitro-5-pentafluorosulfanylbenzoic AcidHCID 178418361HCID 178418361、化合物

生成物 1

HCID 580857063-Amino-5-pentafluorosulfanylbenzoic acid収率 86.9%

試薬・触媒・溶媒 2

HCID 935Nickel触媒HCID 887Methanol溶媒

実験手順

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.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  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)

出典と根拠

ORDレコード
ord-ee0c30554f804d4d80a3598974f0622d
出典データセット
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08198272B2

反応ノート

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