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

Potassium Hydroxide → HCID 21292013, 화합물

HRID 1154704
노트
인쇄 미리보기

반응식

HRID 1154704 반응식
[CH3:1][N:2]([CH2:4][C:5]1[N:10]=[C:9]([O:11][CH2:12][CH2:13][CH2:14][NH:15]C=O)[CH:8]=[CH:7][CH:6]=1)[CH3:3].[OH-].[K+]>CO.C(OCC)C>[CH3:1][N:2]([CH2:4][C:5]1[N:10]=[C:9]([O:11][CH2:12][CH2:13][CH2:14][NH2:15])[CH:8]=[CH:7][CH:6]=1)[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 14797Potassium HydroxideHCID 20434286N-[3-(6-Dimethylaminomethyl-2-pyridyloxy)propyl]formamide

생성물 1

HCID 21292013HCID 21292013, 화합물수율 77.2%

시약·촉매·용매 2

HCID 887Methanol용매HCID 3283Diethyl Ether용매

실험 절차

N-[3-(6-dimethylaminomethyl-2-pyridyloxy) propyl]formamide (2.7 g, 0.013 mol) is added to a solution of 85% potassium hydroxide pellets (3.0 g) dissolved in methanol (30 ml) and heated at gentle reflux for 21 hours. The reaction is cooled, diluted with diethyl ether (30 ml), the precipitated salts filtered, and the solvent removed under vacuum. The residue is dissolved in water and the product exhaustively extracted into ethanol/chloroform, dried and evaporated to give 2.1 g of pure product.

후처리

  1. temperatureheated
  2. temperatureat gentle reflux for 21 hours
  3. temperatureThe reaction is cooled
  4. filtrationthe precipitated salts filtered
  5. customthe solvent removed under vacuum
  6. dissolutionThe residue is dissolved in water
  7. extractionthe product exhaustively extracted into ethanol/chloroform
  8. customdried
  9. customevaporated

출처 및 근거

ORD 기록
ord-c7ef9001d41a4d17b3b8667409eeed9b
출처 데이터셋
uspto-grants-1984_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04490533

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트