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

N-Methyl-4-nitroaniline → 2-bromo-N-methyl-N-(4-nitrophenyl)acetamide

HRID 1374818
노트
인쇄 미리보기

반응식

HRID 1374818 반응식
[CH3:1][NH:2][C:3]1[CH:8]=[CH:7][C:6]([N+:9]([O-:11])=[O:10])=[CH:5][CH:4]=1.C(=O)([O-])[O-].[Li+].[Li+].[Br:18][CH2:19][C:20](Br)=[O:21]>O1CCOCC1>[Br:18][CH2:19][C:20]([N:2]([C:3]1[CH:4]=[CH:5][C:6]([N+:9]([O-:11])=[O:10])=[CH:7][CH:8]=1)[CH3:1])=[O:21]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7483N-Methyl-4-nitroanilineHCID 11125Lithium CarbonateHCID 61147Bromoacetyl bromide

생성물 1

HCID 226683752-bromo-N-methyl-N-(4-nitrophenyl)acetamide

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

실험 절차

23.5 g (0.15 mol) of N-methyl-4-nitroaniline are dissolved in 400 ml of dioxane and combined with 22.2 g (0.3 mol) of lithium carbonate. Then 32.2 g (0.18 mol) of bromoacetylbromide are added dropwise in such a way that the internal temperature does not exceed 33° C. After 18 hours' stirring the reaction solution is evaporated down to 100 ml, combined with 500 ml of water and stirred for 1 hour. The precipitate formed is suction filtered, washed with water and dried. The crude product is stirred in 400 ml of ethyl acetate at 40° C. Then the insoluble matter is filtered off, the solution is evaporated down and the solid residue is triturated with ether.

후처리

  1. customdoes not exceed 33° C
  2. customis evaporated down to 100 ml
  3. stirringstirred for 1 hour
  4. customThe precipitate formed
  5. filtrationfiltered
  6. washwashed with water
  7. customdried
  8. stirringThe crude product is stirred in 400 ml of ethyl acetate at 40° C
  9. filtrationThen the insoluble matter is filtered off
  10. customthe solution is evaporated down
  11. customthe solid residue is triturated with ether

출처 및 근거

ORD 기록
ord-487c1062038b4161a14f69910aadf268
출처 데이터셋
uspto-grants-2007_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07166615B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트