Triphenylphosphine → 1-Bromo-5-trimethylsilylpent-2-en-4-yne

HRID 1671728

Reaktionsgleichung

Reaktionsgleichung von HRID 1671728
[Br:1]N1C(=O)CCC1=O.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[CH3:28][Si:29]([CH3:37])([CH3:36])[C:30]#[C:31]/[CH:32]=[CH:33]/[CH2:34]O>ClCCl>[Br:1][CH2:34][CH:33]=[CH:32][C:31]#[C:30][Si:29]([CH3:37])([CH3:36])[CH3:28]

Komponenten

5

Versuchsvorschrift

N-Bromosuccinimide (85.3 g, 0.48 mol) was added in portions to a nearly homogeneous solution of triphenylphosphine (128.2 g, 0.49 mol) and 2E-5-trimethylsilylpent-2-en-4-yn-1-ol (72.5 g, 0.47 mol) in dichloromethane (600 mL) under nitrogen and cooled in a dry ice/2-propanol bath to an initial temperature of below −20° C. The internal temperature of the reaction mixture was maintained at −10° C. to 0° C. throughout the addition by adjusting the rate of addition. The bath was allowed to warm to ambient temperature. After 2 hours, the reaction was complete. The reaction mixture was concentrated under vacuum to a thick paste and the residue was triturated with hexane (250 mL). The suspension was filtered and the solids and silica gel were rinsed with hexane (10×150 mL). The filtrate was concentrated under vacuum (30° C./60 mtorr) to obtain 44 g (89% yield) of 1-bromo-5-trimethylsilylpent-2-en-4-yne, a compound of formula (P), as a pale yellow oil: 1H-NMR (300 mHz, CDCl3) δ0.19 (s, 9H), 3.95 (d, 2H), 5.75 (d, 1H), 6.31 (dt, 1H) ppm.

Aufarbeitung

  1. temperaturecooled in a dry ice/2-propanol bath to an initial temperature of below −20° C
  2. temperatureThe internal temperature of the reaction mixture was maintained at −10° C. to 0° C. throughout the addition
  3. additionthe rate of addition
  4. concentrationThe reaction mixture was concentrated under vacuum to a thick paste
  5. customthe residue was triturated with hexane (250 mL)
  6. filtrationThe suspension was filtered
  7. washthe solids and silica gel were rinsed with hexane (10×150 mL)
  8. concentrationThe filtrate was concentrated under vacuum (30° C./60 mtorr)

Quellen und Nachweise

ORD-Eintrag
ord-65525c313ed34850b7306c852b1e177c
Quelldatensatz
uspto-grants-2011_08
Patentnummer
US07994346B2

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