Reaktion #5152

ord-8970a9cd79a34b338559a5f59227a0d1

Reaktionsgleichung

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

Lösungsmittel

Reaktionsbedingungen

Temperatur
50°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigean exothermic reaction
  2. 2
    TemperaturHeating
  3. 3
    Sonstigewas continued at 100° C.
  4. 4
    Sonstige(1 h), and 150° C. (2.5 h)
  5. 5
    workup.DISTILLATIONDistillation

Vorschrift

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.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05243025uspto-grants-1993_09