Chlorotrimethylsilane → 3,9-Dioxa-2,10-disilaundecane, 2,2,10,10-tetramethyl-

Temperatur

50 °C

1,5-Pentanediol (65 g, 0.62 tool) 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 tool 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 NPIR (CDCl3): 3.60 (t, J=7Hz, 4H), 1.57 (m, 4H), 1.40 (m, 2H), 0.12 (s, 18H), consistent With the assigned structure.

1. customan exothermic reaction
2. temperatureHeating
3. customwas continued at 100° C.
4. custom(1 h), and 150° C. (2.5 h) GC analysis (method 1)
5. distillationDistillation

ORD-Eintrag

ord-927081513db547d38fa339f8090715b5

Quelldatensatz

uspto-grants-1995_10

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US05457215