Реакция #2075684

ord-0ad76da21683406aa700df16e455a575

Уравнение реакции

CCN(CC)CC
triethylamine
CCCCC/C=C\C/C=C\CCCCCCCCO
Linoleyl alcohol
CS(=O)(=O)Cl
Methanesulfonyl chloride
CCCCC/C=C\C/C=C\CCCCCCCCOS(C)(=O)=O
colorless oil
Выход 97.0%
CCCCC/C=C\C/C=C\CCCCCCCCOS(C)(=O)=O
Linoleyl mesylate
Выход 97.0%

Растворители

Условия реакции

Температура
0°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеThe flask was sealed
  2. 2
    Другоеflushed with argon
  3. 3
    workup.ADDITIONadded slowly to the stirring reaction mixture
  4. 4
    Промывкаwashed with saturated bicarbonate solution (2×200 mL)
  5. 5
    СушкаThe organic phase was dried over MgSO4
  6. 6
    Фильтрацияfiltered
  7. 7
    Концентрированиеconcentrated

Методика

Linoleyl alcohol (10.0 g, 37.5 mmol) was weighed into a 500 mL round bottomed flask with a stir bar. The flask was sealed, flushed with argon, charged with DCM (100 mL) and triethylamine (7.84 mL, 1.5 equiv.) and cooled to 0° C. Methanesulfonyl chloride (4.35 mL), 1.5 equiv.) was measured in a PP syringe and added slowly to the stirring reaction mixture. TLC analysis (7.5% EtOAc/Hexanes) showed the reaction was complete within 1 hr. The reaction was diluted with DCM (100 mL) and washed with saturated bicarbonate solution (2×200 mL). The organic phase was dried over MgSO4, filtered and concentrated to give 12.53 g (97%) of colorless oil that was used without further purification.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07641915B2uspto-grants-2010_01