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

1,1-Bis(methylthio)-2-nitroethylene → 2-(Nitromethylene)-1-((tetrahydrofuran-3-yl)methyl)imidazolidine

HRID 1441388
노트
인쇄 미리보기

반응식

HRID 1441388 반응식
CS[C:3](SC)=[CH:4][N+:5]([O-:7])=[O:6].[O:10]1[CH2:14][CH2:13][CH:12]([CH2:15][NH:16][CH2:17][CH2:18][NH2:19])[CH2:11]1>C(O)C>[N+:5]([CH:4]=[C:3]1[NH:19][CH2:18][CH2:17][N:16]1[CH2:15][CH:12]1[CH2:13][CH2:14][O:10][CH2:11]1)([O-:7])=[O:6]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 836231,1-Bis(methylthio)-2-nitroethyleneHCID 59164401N1-((tetrahydrofuran-3-yl)methyl)ethane-1,2-diamine

생성물 1

HCID 668310512-(Nitromethylene)-1-((tetrahydrofuran-3-yl)methyl)imidazolidine수율 81%

시약·촉매·용매 1

HCID 702Ethanol용매

반응 조건

온도
85 °C

실험 절차

2.5 g (0.0178 mol) of 1,1-dimethylthio-2-nitroethene, 2.56 g (0.0178 mol) of N1-((tetrahydrofuran-3-yl)methyl)ethane-1,2-diamine were added to 50 ml of ethanol. The resulting mixture was heated under reflux for 8 hours at 80-90 ° C. The mixture was then cooled to educe solid, concentrated, filtrated and dried to give a light yellow powder in 81% yield.

후처리

  1. temperatureThe resulting mixture was heated
  2. temperatureThe mixture was then cooled
  3. concentrationconcentrated
  4. filtrationfiltrated
  5. customdried
  6. customto give a light yellow powder in 81% yield

출처 및 근거

ORD 기록
ord-e5ce06ae61b443f3858006c68e49ba9c
출처 데이터셋
uspto-grants-2010_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07655665B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트