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

Hydroxyamine hydrochloride → 2-(3,4-Dimethoxyphenoxy)-N'-hydroxyacetoimidamide

HRID 710048
노트
인쇄 미리보기

반응식

HRID 710048 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:10]=[CH:11][C:12]=1[O:13][CH3:14])[O:6][CH2:7][C:8]#[N:9].Cl.[OH:16][NH2:17]>CO.O>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:10]=[CH:11][C:12]=1[O:13][CH3:14])[O:6][CH2:7][C:8](=[N:17][OH:16])[NH2:9]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 443297Hydroxyamine hydrochlorideHCID 189913533,4-Dimethoxyphenoxyacetonitrile

생성물 1

HCID 867067612-(3,4-Dimethoxyphenoxy)-N'-hydroxyacetoimidamide

시약·촉매·용매 1

HCID 22242641Methanol--water (1/1)용매

반응 조건

온도
100 °C

실험 절차

To a solution of 2-(3,4-dimethoxyphenoxy)acetonitrile (3.8 g) in MeOH—H2O (1:1), hydroxyamine hydrochloride was added and the mixture was stirred at 100° C. for 3 hours. After distilling off the solvent under reduced pressure, the residue was recovered by filtration and washed with water and hexane to give a crude form of the titled compound (4.9 g).

후처리

  1. distillationAfter distilling off the solvent under reduced pressure
  2. filtrationthe residue was recovered by filtration
  3. washwashed with water and hexane

출처 및 근거

ORD 기록
ord-9ca000f3a7e144bdbd9b052e1308891e
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09181229B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트