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Ammonium Persulfate → HCID 22117145, 화합물

HRID 1275539
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HRID 1275539 반응식
[C:1]([O:9][C:10]1[C:11](=[O:21])[C:12]2[C:17]([C:18](=[O:20])[CH:19]=1)=[CH:16][CH:15]=[CH:14][CH:13]=2)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH3:22][Si:23]([CH:26](C)[C:27](O)=O)([CH3:25])[CH3:24].S(OOS([O-])(=O)=O)([O-])(=O)=O.[NH4+].[NH4+]>C(#N)C.O.C(OCC)C.[N+]([O-])([O-])=O.[Ag+]>[C:1]([O:9][C:10]1[C:11](=[O:21])[C:12]2[C:17]([C:18](=[O:20])[C:19]=1[CH2:27][CH2:26][Si:23]([CH3:25])([CH3:24])[CH3:22])=[CH:16][CH:15]=[CH:14][CH:13]=2)(=[O:8])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 3

HCID 62648Ammonium PersulfateHCID 825051HCID 825051, 화합물HCID 12218619HCID 12218619, 화합물

생성물 1

HCID 22117145HCID 22117145, 화합물수율 46.4%

시약·촉매·용매 4

HCID 24470Silver Nitrate촉매HCID 962Water용매
HCID 3283
Diethyl Ether
용매
HCID 6342Acetonitrile용매

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온도
65 °C

실험 절차

2-Benzoyloxy-1,4-naphthoquinone (1.39 g, 5 mmol), trimethylsilylpropionic acid (1.09 g, 7.5 mmol) and silver nitrate (523 mg, 3 mmol) were suspended in 40 ml aqueous acetonitrile (1:1) and then heated to 65° C. Ammonium persulphate (1.71 g, 7.5 mmol) in 20 ml water was added slowly and dropwise over 30 minutes to the mixture. The reaction mixture was stirred at this temperature for a further hour and then cooled, diluted with diethyl ether and the aqueous phase removed. The organic extract was washed with saturated sodium bicarbonate solution, then brine and dried over anhydrous magnesium sulphate. After concentration in vacuo, the crude material was chromatographed using petroleum ether/ethyl acetate as eluent to give 2-benzoyloxy-3-(2'-trimethylsilylethyl)-1,4-naphthoquinone (879 mg) which was recrystallised from methanol, m.pt.: 92-95° C. NMR peaks at: 184.4, 178.2, 150.3, 142.6, 134.0, 133.8, 132.1, 130.9, 126.6, 126.6; 18.8, 16.2; -2.0; 163.8, 128.0, 128.7, 130.4, 134.2 (PhCO).

후처리

  1. temperaturecooled
  2. customthe aqueous phase removed
  3. extractionThe organic extract
  4. washwas washed with saturated sodium bicarbonate solution
  5. dry with materialbrine and dried over anhydrous magnesium sulphate
  6. concentrationAfter concentration in vacuo
  7. customthe crude material was chromatographed

출처 및 근거

ORD 기록
ord-e68e4fa1be104e00b5ec9c0d5fb52ed6
출처 데이터셋
uspto-grants-2000_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06162799

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