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4-nitrophenyl 1,5-dithio-beta-D-xylopyranoside → 4-aminophenyl 1,5-dithio-beta-D-xylopyranoside

HRID 6025
ノート
印刷プレビュー

反応式

HRID 6025 の反応式
[S:1]([C:11]1[CH:16]=[CH:15][C:14]([N+:17]([O-])=O)=[CH:13][CH:12]=1)[C@@H:2]1[S:10][CH2:9][C@@H:7]([OH:8])[C@H:5]([OH:6])[C@H:3]1[OH:4]>CO.[Pd]>[S:1]([C:11]1[CH:12]=[CH:13][C:14]([NH2:17])=[CH:15][CH:16]=1)[C@@H:2]1[S:10][CH2:9][C@@H:7]([OH:8])[C@H:5]([OH:6])[C@H:3]1[OH:4]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 1

HCID 147953714-nitrophenyl 1,5-dithio-beta-D-xylopyranoside

生成物 1

HCID 538154504-aminophenyl 1,5-dithio-beta-D-xylopyranoside収率 46%

試薬・触媒・溶媒 2

HCID 23938Palladium触媒2 回HCID 887Methanol溶媒

実験手順

170 mg of 10% palladium-on-charcoal are added to a solution of 1.7 g (5.61.10-3 mol) of 4-nitrophenyl 1,5-dithio-β-D-xylopyranoside in 150 ml of methanol. The reaction medium is kept under hydrogen pressure (3.5.105Pa) at room temperature for 3 days. Repeat amounts of 170 mg of 10% palladium-on-charcoal are added after stirring for 3 hours, 4 hours, 12 hours and 24 hours. The mixture obtained is filtered, the solvent is evaporated off under reduced pressure and the residue obtained is purified by flash chromatography using a CHCl3 /CH3OH mixture (9/1 v/v) as the eluent, and is then recrystallized from water to give 0.7 g (yield: 46%) of the expected product.

後処理

  1. customat room temperature
  2. customfor 3 days
  3. additionare added
  4. customThe mixture obtained
  5. filtrationis filtered
  6. customthe solvent is evaporated off under reduced pressure
  7. customthe residue obtained
  8. customis purified by flash chromatography
  9. customis then recrystallized from water

出典と根拠

ORDレコード
ord-27586a11f84249d2aead91f87b678a79
出典データセット
uspto-grants-1993_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05246961

反応ノート

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