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

HRID 5056

반응식

HRID 5056 반응식
[CH2:1]([OH:7])[CH2:2][CH2:3][CH2:4][CH2:5][OH:6].[CH3:8][Si:9](Cl)([CH3:11])[CH3:10]>C[Si](N[Si](C)(C)C)(C)C>[Si:9]([O:6][CH2:5][CH2:4][CH2:3][CH2:2][CH2:1][O:7][Si:9]([CH3:11])([CH3:10])[CH3:8])([CH3:11])([CH3:10])[CH3:8]

참가 물질

4

반응물 2

HCID 6397ChlorotrimethylsilaneHCID 81051,5-Pentanediol

생성물 1

HCID 1431753,9-Dioxa-2,10-disilaundecane, 2,2,10,10-tetramethyl-

시약·촉매·용매 1

HCID 13838Hexamethyldisilazane용매3회

반응 조건

온도
50 °C

실험 절차

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.

후처리

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

출처 및 근거

ORD 기록
ord-8970a9cd79a34b338559a5f59227a0d1
출처 데이터셋
uspto-grants-1993_09
특허 번호
US05243025

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