홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

1,3-Butadiene → 1,1-Dichloro-1-silacyclo-3-pentene

HRID 1583088
노트
인쇄 미리보기

반응식

HRID 1583088 반응식
C=CC=C.Cl[SiH](Cl)Cl.[Cl:9][Si:10]([Cl:20])([Cl:19])[CH2:11][CH:12]=[CH:13][CH2:14][Si](Cl)(Cl)Cl>[Cl-].C([P+](CCCC)(CCCC)CCCC)CCC>[CH2:14]1[Si:10]([Cl:20])([Cl:19])[CH2:11][CH:12]=[CH:13]1.[CH2:11]([Si:10]([Cl:20])([Cl:19])[Cl:9])[CH:12]=[CH:13][CH3:14]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 78451,3-ButadieneHCID 24811TrichlorosilaneHCID 53686027HCID 53686027, 화합물

생성물 2

HCID 1366721,1-Dichloro-1-silacyclo-3-pentene수율 68%HCID 543214Crotyltrichlorosilane수율 20%

시약·촉매·용매 1

HCID 75311
Tetrabutylphosphonium chloride
촉매

반응 조건

온도
150 °C

실험 절차

In a a 25 ml oven dried stainless steel tube ,1,3-butadiene (1.27 g, 23.26 mmol), trichlorosilane (14.7 g, 108.53 mmol) and tetrabutylphosphonium chloride (0.68 g, 2.31 mmol) were added under a dry nitrogen atmosphere. After sealing the cylinder with a cap, the reactor was maintained at 150° C. for 2 hours. The resulting mixture was distilled to yield 2.44 g (yield: 68%) of 1,1-dichlorosilacyclo-3-pentene main product, 0.88 g (yield: 20%) of crotyltrichlorosilane by product, and 0.37 g (yield: 5%) of trace 1,4-bis(trichlorosilyl)-2-butene.

후처리

  1. distillationThe resulting mixture was distilled

출처 및 근거

ORD 기록
ord-0ee3451c15c242fcb1570e666a6e7e96
출처 데이터셋
uspto-grants-2004_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06740766B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트