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Hydrogen Bromide → Phytanyl Bromide

HRID 2304131
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HRID 2304131 반응식
[CH3:1][CH:2]([CH2:6][CH2:7][CH2:8][CH:9]([CH3:21])[CH2:10][CH2:11][CH2:12][CH:13]([CH3:20])[CH2:14][CH2:15][CH2:16][CH:17]([CH3:19])[CH3:18])[CH2:3][CH2:4]O.[BrH:22].S(=O)(=O)(O)O>O>[Br:22][CH2:4][CH2:3][CH:2]([CH3:1])[CH2:6][CH2:7][CH2:8][CH:9]([CH3:21])[CH2:10][CH2:11][CH2:12][CH:13]([CH3:20])[CH2:14][CH2:15][CH2:16][CH:17]([CH3:19])[CH3:18]
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참가 물질

5

반응물 3

HCID 260Hydrogen BromideHCID 1118Sulfuric AcidHCID 102459Dihydrophytol

생성물 1

HCID 10808570Phytanyl Bromide수율 84%

시약·촉매·용매 1

HCID 962Water용매

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온도
100 °C

실험 절차

To a mixture of 40.0 g (134 mmol) of 3,7,11,15-tetramethyl-1-hexadecanol and 400 mL of 48% hydrobromic acid was slowly added 40 mL of concentrated sulfuric acid. The reaction mixture was heated at 100° C. for 24 h and poured into 1.2 L of water. The mixture was extracted with hexanes, and the combined organic phases were washed with saturated aqueous NaHCO3 and dried over MgSO4. The solution was concentrated to a dark liquid, which was eluted through 3 inches (7.6 cm) of silica with hexanes. Concentration of the eluent yielded a light amber liquid, and bulb-to-bulb distillation gave 40.8 g (84%) of 1-bromo-3,7,11,15-tetramethylhexadecane as a clear, colorless liquid, bp 160-180° C. at 0.06 mm Hg.

후처리

  1. extractionThe mixture was extracted with hexanes
  2. washthe combined organic phases were washed with saturated aqueous NaHCO3
  3. dry with materialdried over MgSO4
  4. concentrationThe solution was concentrated to a dark liquid, which
  5. washwas eluted through 3 inches (7.6 cm) of silica with hexanes
  6. customConcentration of the eluent yielded
  7. distillationa light amber liquid, and bulb-to-bulb distillation

출처 및 근거

ORD 기록
ord-f2b3b1e832d64103b32b6ac9afeb4558
출처 데이터셋
uspto-grants-2002_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06433359B1

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