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tert-Butyl hydroperoxide → HCID 53631979, 화합물

HRID 1590935
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HRID 1590935 반응식
[C:1]([O:22][CH:23]1[CH2:28][C:27]([CH3:30])([CH3:29])[NH:26][C:25]([CH3:32])([CH3:31])[CH2:24]1)(=[O:21])[C:2]1[C:3](=[CH:17][CH:18]=[CH:19][CH:20]=1)[C:4]([O:6][CH:7]1[CH2:12][C:11]([CH3:14])([CH3:13])[NH:10][C:9]([CH3:16])([CH3:15])[CH2:8]1)=[O:5].[C:33]([O:37]O)([CH3:36])([CH3:35])C>[Mo](=O)(=O)=O.C1CCCCC1>[C:4]([O:6][CH:7]1[CH2:8][C:9]([CH3:16])([CH3:15])[N:10]([O:37][CH:33]2[CH2:36][CH2:17][CH2:3][CH2:4][CH2:35]2)[C:11]([CH3:13])([CH3:14])[CH2:12]1)(=[O:5])[C:3]1[C:2](=[CH:20][CH:19]=[CH:18][CH:17]=1)[C:1]([O:22][CH:23]1[CH2:24][C:25]([CH3:32])([CH3:31])[N:26]([O:37][CH:33]2[CH2:36][CH2:20][CH2:2][CH2:1][CH2:35]2)[C:27]([CH3:30])([CH3:29])[CH2:28]1)=[O:21]
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참가 물질

5

반응물 2

HCID 6410tert-Butyl hydroperoxide3회HCID 1513129Bis(2,2,6,6-tetramethyl-4-piperidinyl) phthalate

생성물 1

HCID 53631979HCID 53631979, 화합물수율 143.3%

시약·촉매·용매 2

HCID 14802Molybdenum trioxide촉매HCID 8078Cyclohexane용매

반응 조건

온도
140 °C

실험 절차

A mixture of 30.0 g (67.5 mmol) of di-(2,2,6,6-tetramethyl-piperidin-4-yl) phthalate, 27.5 g (214 mmol) of 70% aqueous t-butyl hydroperoxide, 2.0 g of molybdenum trioxide, and 200 ml of cyclohexane is heated to reflux. Water is collected in a Dean-Stark trap. After 75 min., the reaction mixture becomes red. Another portion of t-butyl hydroperoxide (42.5 g, 70%, 330 mmol) is added over 30 minutes. After the additional water is collected, the reaction mixture is transferred to a Fischer-Porter bottle and heated at 140° C. for 4.5 hours. The nearly colorless reaction mixture is treated with 6.9 g (90%, 69 mmol) of t-butyl hydroperoxide and heated at 140° C. for 90 minutes to remove the last traces of pink color. The reaction mixture is cooled, filtered, and stirred with a solution of 43 g of sodium sulfite in 530 ml of water for 2 hours. Dichloromethane (600 ml) is added, and the organic layer is separated, dried over magnesium sulfate, and concentrated to obtain a crude solid. Purification (Waters Prep. 500A HPLC, 25:1 heptane:ethyl acetate) affords 31.0 g (72% yield) of a white solid, m.p. 149°-51° C.

후처리

  1. temperatureis heated to reflux
  2. customWater is collected in a Dean-Stark trap
  3. customAfter the additional water is collected
  4. temperatureheated at 140° C. for 90 minutes
  5. customto remove the last traces of pink color
  6. temperatureThe reaction mixture is cooled
  7. filtrationfiltered
  8. additionDichloromethane (600 ml) is added
  9. customthe organic layer is separated
  10. dry with materialdried over magnesium sulfate
  11. concentrationconcentrated
  12. customto obtain a crude solid
  13. customPurification (Waters Prep. 500A HPLC, 25:1 heptane:ethyl acetate)

출처 및 근거

ORD 기록
ord-4fc763e57fd743adad48425debc9828b
출처 데이터셋
uspto-grants-1993_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05204473

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