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

Sodium Sulfate → 2,2-Dimethyl-5-(2-(2-(dimethylamino)ethoxy)ethyl-imino)-3-hexanone

HRID 551716
노트
인쇄 미리보기

반응식

HRID 551716 반응식
[CH3:1][C:2]([CH3:10])([C:4](=[O:9])[CH2:5][C:6](=O)[CH3:7])[CH3:3].[CH3:11][N:12]([CH3:19])[CH2:13][CH2:14][O:15][CH2:16][CH2:17][NH2:18].S([O-])([O-])(=O)=O.[Na+].[Na+]>C(OCC)C>[CH3:1][C:2]([CH3:10])([C:4](=[O:9])[CH2:5][C:6](=[N:18][CH2:17][CH2:16][O:15][CH2:14][CH2:13][N:12]([CH3:19])[CH3:11])[CH3:7])[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 24436Sodium SulfateHCID 817415,5-Dimethylhexane-2,4-dioneHCID 22322041(2-(2-Aminoethoxy)ethyl)dimethylamine

생성물 1

HCID 866158372,2-Dimethyl-5-(2-(2-(dimethylamino)ethoxy)ethyl-imino)-3-hexanone

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

In a 100 mL round bottom flask equipped with a magnetic stirrer, 8 g 2,2-dimethylhexane-3,5-dione was combined with 1.1 equivalents of 2-(2-(dimethylamino)ethoxy)ethylamine, anhydrous sodium sulfate and anhydrous diethyl ether and stirred over three days under nitrogen. The ether was removed on a rotary evaporator and the residue was vacuum distilled through a Vigreux column to yield 9.7 g of product.

후처리

  1. customIn a 100 mL round bottom flask equipped with a magnetic stirrer
  2. customThe ether was removed on a rotary evaporator
  3. distillationdistilled through a Vigreux column

출처 및 근거

ORD 기록
ord-b7e2ec1a87834682a9324d26ab859363
출처 데이터셋
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07947814B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트