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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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4-nitrophenyl 1,5-dithio-beta-D-xylopyranoside → 4-aminophenyl 1,5-dithio-beta-D-xylopyranoside

HRID 2372989
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HRID 2372989 반응식
[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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

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

생성물 1

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

시약·촉매·용매 2

HCID 23938Palladium촉매2회HCID 887Methanol용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-c06640951a8e4f80aa69752058269adf
출처 데이터셋
uspto-grants-1992_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05101048

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