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Water → 1-(9,10-dihydroxydecyl)-3,7-dimethylxanthine

HRID 1756269
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HRID 1756269 반응식
[CH2:1]([N:11]1[C:20](=[O:21])[C:19]2[N:18]([CH3:22])[CH:17]=[N:16][C:15]=2[N:14]([CH3:23])[C:12]1=[O:13])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH:9]=[CH2:10].C[N+]1([O-])CC[O:28]CC1.[OH2:32].S(S([O-])=O)([O-])=O.[Na+].[Na+]>CC(O)(C)C.CC(C)=O.O=[Os](=O)(=O)=O>[OH:32][CH:9]([CH2:10][OH:28])[CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2][CH2:1][N:11]1[C:20](=[O:21])[C:19]2[N:18]([CH3:22])[CH:17]=[N:16][C:15]=2[N:14]([CH3:23])[C:12]1=[O:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 4

HCID 962WaterHCID 24489Sodium DithioniteHCID 82029Methyl morpholine oxideHCID 15230636HCID 15230636, 화합물

생성물 1

HCID 98198951-(9,10-dihydroxydecyl)-3,7-dimethylxanthine수율 93%

시약·촉매·용매 3

HCID 30318Osmium Tetroxide
촉매
HCID 180Acetone용매
HCID 6386tert-Butanol용매

실험 절차

A solution of (1-(9-decenyl)-3,7-dimethylxanthine (3.2 g, 10.1 mmol)), 4-methylmorpholine-N-oxide (1.41 g, 12 mmol) and OsO4 (3 drops of a 2.5% solution by weight in tBuOH) in acetone (40 ml) and water (10 ml) was stirred for 24 hrs. A saturated solution of sodium dithionite (5 ml) was added to the reaction mixture which was then stirred for 15 min. The reaction mixture was extracted with 25 % EtOH/dichloromethane (4×50 ml). The organic layers were combined, dried with sodium sulfate and evaporated to a white solid which was recrystalized in ethanol to give 1-(9,10-dihydroxydecyl)-3,7-dimethylxanthine (3.30 g, 93% yield).

후처리

  1. extractionThe reaction mixture was extracted with 25 % EtOH/dichloromethane (4×50 ml)
  2. dry with materialdried with sodium sulfate
  3. customevaporated to a white solid which
  4. customwas recrystalized in ethanol

출처 및 근거

ORD 기록
ord-201cda1531f24af580928d67435cc4e5
출처 데이터셋
uspto-grants-1995_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05440041

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