Реакция #1121725

ord-7a9a6543c7a54595b60f0a16b7c2ff4d

Уравнение реакции

O
water
CN(C)CC(O)CO
3-(dimethylamino)-1,2-propanediol
c1c[nH]cn1
imidazole
CC(C)(C)[Si](C)(C)Cl
tert-butyldimethylsilyl chloride
CN(C)CC(O)CO[Si](C)(C)C(C)(C)C
1-(tert-butyldimethylsilyloxy)-3-(dimethylamino)propan-2-ol

Растворители

Условия реакции

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

Обработка

  1. 1
    ДругоеThe organic layer was separated
  2. 2
    Экстракцияthe aqueous layer was extracted with two additional portions of dichloromethane (20 mL)
  3. 3
    СушкаThe combined organic extracts were dried (MgSO4)
  4. 4
    Фильтрацияfiltered
  5. 5
    Концентрированиеconcentrated

Методика

A dry dichloromethane (10 mL) solution of 3-(dimethylamino)-1,2-propanediol (98%, 1.00 g, 8.39 mmol, 1.0 equiv) and imidazole (0.57 g, 8.39 mmol, 1.0 equiv) was stirred at 0° C. under argon for 15 minutes. Solid tert-butyldimethylsilyl chloride (1.26 g, 8.39 mmol, 1.0 equiv) was added to the mixture and the resultant was stirred for 2 hours at 0° C. The mixture was then diluted with 20 mL of dichloromethane and poured into deionized water (15 mL). The organic layer was separated and the aqueous layer was extracted with two additional portions of dichloromethane (20 mL). The combined organic extracts were dried (MgSO4), filtered and concentrated to afford crude 1-(tert-butyldimethylsilyloxy)-3-(dimethylamino)propan-2-ol, a thick clear oil, which was used without further purification.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08545877B2uspto-grants-2013_10