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

Iodoacetamide → 2-(2-Nitrophenoxy)acetamide

HRID 863248
노트
인쇄 미리보기

반응식

HRID 863248 반응식
C(=O)([O-])[O-].[K+].[K+].I[CH2:8][C:9]([NH2:11])=[O:10].[N+:12]([C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=1[OH:21])([O-:14])=[O:13]>CC(C)=O>[C:9]([CH2:8][O:21][C:16]1[CH:17]=[CH:18][CH:19]=[CH:20][C:15]=1[N+:12]([O-:14])=[O:13])(=[O:10])[NH2:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 3727IodoacetamideHCID 69472-NitrophenolHCID 11430Potassium Carbonate

생성물 1

HCID 49318272-(2-Nitrophenoxy)acetamide

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

8.0 g of potassium carbonate and 11.4 g of iodoacetamide are added to a solution of 4.0 g of 2-nitrophenol in 50 ml acetone. The reaction mixture is heated under reflux for 7 h and then concentrated. The residue is dissolved in chloroform and extracted with 0.05N of sodium hydroxide solution. Recyrstallization of the crude product from tetrahydrofuran gives 2-(carbamoylmethoxy)nitrobenzene of mp 190°-1° C.; Rf (O)=0.55.

후처리

  1. temperatureThe reaction mixture is heated
  2. temperatureunder reflux for 7 h
  3. concentrationconcentrated
  4. dissolutionThe residue is dissolved in chloroform
  5. extractionextracted with 0.05N of sodium hydroxide solution

출처 및 근거

ORD 기록
ord-3dc3f48d9b5549fc99e00f009cf9de65
출처 데이터셋
uspto-grants-1998_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05719141

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트