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Acrylonitrile → 1-t-Butyldimethylsilyl-4-(2-cyanoethyl)piperazine

HRID 590534
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인쇄 미리보기

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HRID 590534 반응식
[Si:1]([N:8]1[CH2:13][CH2:12][NH:11][CH2:10][CH2:9]1)([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2].[C:14](#[N:17])[CH:15]=[CH2:16]>>[Si:1]([N:8]1[CH2:13][CH2:12][N:11]([CH2:16][CH2:15][C:14]#[N:17])[CH2:10][CH2:9]1)([C:4]([CH3:7])([CH3:5])[CH3:6])([CH3:3])[CH3:2]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 7855AcrylonitrileHCID 19434780Tert-butyl-dimethyl-piperazin-1-ylsilane

생성물 1

HCID 1317344831-t-Butyldimethylsilyl-4-(2-cyanoethyl)piperazine

반응 조건

온도
70 °C

실험 절차

A flask equipped with a stirrer, reflux condenser, dropping funnel and thermometer was charged with 160.3 g (0.8 mol) of 1-t-butyldimethylsilylpiperazine (Synthesis Example 1) and heated at 70° C. Once the internal temperature became steady, 46.7 g (0.88 mol) of acrylonitrile was added dropwise over 2 hours. Stirring was continued for 4 hours at the temperature. On distillation of the reaction solution, 194.1 g of a fraction having a boiling point of 145-147° C./0.4 kPa was collected.

후처리

  1. customA flask equipped with a stirrer
  • temperaturereflux condenser
  • distillationOn distillation of the reaction solution, 194.1 g of a fraction
  • customwas collected
  • 출처 및 근거

    ORD 기록
    ord-bf16fe976ebc46df9931b65748cec9e4
    출처 데이터셋
    uspto-grants-2016_01
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US09233988B2

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