Реакция #86484

ord-fc05b04f677e40c5994d7bc155187ab9

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.ADDITIONwas added
  2. 2
    ЭкстракцияThe aqueous layer was extracted with ether three times
  3. 3
    СушкаThe combined organic layer was dried over MgSO4
  4. 4
    Другоеevaporated
  5. 5
    Другоеwas dried under high vacuum

Методика

2-(methylamino)ethanol (1.0 g, 13.3 mmol) was stirred in DCM (25.0 ml) under atmosphere of nitrogen. DIEA (3.23 ml, 18.6 mmol) followed by tert-butylchlorodimethylsilane (2.0 g, 13.3 mmol) was added and the reaction mixture was stirred at room temperature over night. The reaction mixture was poured into ether/water. The aqueous layer was extracted with ether three times. The combined organic layer was dried over MgSO4 and evaporated and remaining material was dried under high vacuum to afford title compound (1.4 g, yield: 56%). 1H-NMR (400 MHz, CDCl3) δ 0.08 (s, 6H) 0.91 (s, 9H) 1.93 (br. s., 1H) 2.48 (s, 3H) 2.71 (t, 2H) 3.75 (t, 2H).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US09434697B2uspto-grants-2016_09