Reacción #5152

ord-8970a9cd79a34b338559a5f59227a0d1

Ecuación de reacción

OCCCCCO
1,5-Pentanediol
C[Si](C)(C)Cl
trimethylsilyl chloride
C[Si](C)(C)OCCCCCO[Si](C)(C)C
colorless oil
C[Si](C)(C)OCCCCCO[Si](C)(C)C
(CH3)3SiO(CH2)5OSi(CH3)3

Reactivos

Ninguno

Disolventes

Condiciones de reacción

Temperatura
50°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroan exothermic reaction
  2. 2
    TemperaturaHeating
  3. 3
    Otrowas continued at 100° C.
  4. 4
    Otro(1 h), and 150° C. (2.5 h)
  5. 5
    workup.DISTILLATIONDistillation

Procedimiento

1,5-Pentanediol (65 g, 0.62 mol) was placed in a 500 mL 3-necked RB flask and treated with 0.4 mL trimethylsilyl chloride. A portion of HMDS (ca. 20 mL) was added, and an exothermic reaction took place as the mixture became homogeneous. The remainder of the HMDS (130 mL, 0.71 mol total) was added at a controlled rate (ca. 3-5 mL/min), maintaining the reaction temperature at ca. 50° C. Heating was continued at 100° C. (1 h), and 150° C. (2.5 h). GC analysis (method 1) revealed excess HMDS and one product. Distillation provided 139 g of colorless oil, bp 47°-49° C./0.1 mm. 1H NMR (CDCl3): 3.60 (t, J=7Hz, 4H), 1.57 (m, 4H), 1.40 (m, 2H), 0.12 (s, 18H), consistent with the assigned structure.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05243025uspto-grants-1993_09