Reacción #1121725

ord-7a9a6543c7a54595b60f0a16b7c2ff4d

Ecuación de reacción

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

Condiciones de reacción

Temperatura
0°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe organic layer was separated
  2. 2
    Extracciónthe aqueous layer was extracted with two additional portions of dichloromethane (20 mL)
  3. 3
    SecadoThe combined organic extracts were dried (MgSO4)
  4. 4
    Filtraciónfiltered
  5. 5
    Concentraciónconcentrated

Procedimiento

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.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08545877B2uspto-grants-2013_10