Benzyl Bromide → ((Pent-4-yn-1-yloxy)methyl)benzene

HRID 1522999노트

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HRID 1522999 반응식
[H-].[Na+].[C:3]([OH:8])#[C:4][CH2:5][CH2:6][CH3:7].[CH:9]1[CH:14]=[CH:13][C:12]([CH2:15]Br)=[CH:11][CH:10]=1>C1COCC1>[CH2:3]([O:8][CH2:15][C:12]1[CH:13]=[CH:14][CH:9]=[CH:10][CH:11]=1)[CH2:4][CH2:5][C:6]#[CH:7]

참가 물질

5

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온도
0 °C

실험 절차

To a flame-dried round-bottomed flask was added NaH (2 equiv., 47.6 mmol, 1.9 g of a 60% dispersion in mineral oil). The solid was washed with hexanes (15 mL), THF (95 mL) was added and the suspension was cooled to 0° C. Pentynol (1 equiv., 23.8 mmol, 2.0 g) was added drop wise in THF (5 mL), followed by drop wise addition of BnBr (0.92 equiv., 21.9 mmol, 2.60 mL). The reaction was warmed to ambient temperature over 16 h, quenched with saturated aqueous NH4Cl (25 mL), and diluted with water (20 mL). The organic layer was extracted with EtOAc (2×40 mL), washed with brine (40 mL) and dried with Na2SO4. Product isolation was achieved by concentration in vacuo and purification by flash column chromatography to afford ((pent-4-yn-1-yloxy)methyl)benzene (3.60 g, 20.7 mmol, 94%). TLC Rf=0.41 (5% EtOAc/Hex); 1HNMR (300 MHz): δ 7.29-7.44 (5H), 4.55 (s, 2H), 3.61 (t, 2H, J=6.2 Hz), 2.36 (td, 2H, J=7.1, 2.6 Hz), 1.97 (t, 1H, J=2.6 Hz), 1.81-1.93 (m, 2H). 13CNMR (75 MHz): δ 138.5, 128.4, 127.63, 127.58, 84.0, 73.0, 68.7, 68.5, 28.7, 15.3.

후처리

  1. washThe solid was washed with hexanes (15 mL), THF (95 mL)
  2. additionwas added
  3. temperatureThe reaction was warmed to ambient temperature over 16 h
  4. customquenched with saturated aqueous NH4Cl (25 mL)
  5. additiondiluted with water (20 mL)
  6. extractionThe organic layer was extracted with EtOAc (2×40 mL)
  7. washwashed with brine (40 mL)
  8. dry with materialdried with Na2SO4
  9. concentrationProduct isolation was achieved by concentration in vacuo and purification by flash column chromatography

출처 및 근거

ORD 기록
ord-1c270ea69f4a471898ae4bfccba67568
출처 데이터셋
uspto-grants-2015_07
특허 번호
US09079835B2

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