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

Acetic Acid → 2-Bromo-4,6-dimethylaniline

HRID 252680
노트
인쇄 미리보기

반응식

HRID 252680 반응식
[CH3:1][C:2]1[CH:8]=[C:7]([CH3:9])[CH:6]=[CH:5][C:3]=1[NH2:4].C(O)(=O)C.[Br:14]Br>>[Br:14][C:5]1[CH:6]=[C:7]([CH3:9])[CH:8]=[C:2]([CH3:1])[C:3]=1[NH2:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 176Acetic AcidHCID 72502,4-DimethylanilineHCID 24408Bromine

생성물 1

HCID 1705792-Bromo-4,6-dimethylaniline

실험 절차

To a solution of 50.0 g (0.413 mol) of 2,4-dimethylaniline in 1500 cm3 of glacial acetic acid 21.2 ml (65.6 g, 0.410 mol) of bromine was added dropwise while vigorously stirring for ca. 20 min. This mixture was stirred for 2 h at 40° C. The precipitate formed was filtered off, washed with 50 ml of acetic acid, and dried in air. Then, this white solid was added to a solution of 100 g of potassium hydroxide in 400 ml of water. This mixture was stirred for 30 min. The crude product was extracted with 3×100 ml of dichloromethane. The combined extract was dried over Na2SO4 and evaporated to dryness. Fractional distillation gave a yellowish liquid, bp 83-85° C./1 mm Hg. Yield 46.9 g (57%).

후처리

  1. stirringThis mixture was stirred for 2 h at 40° C
  2. customThe precipitate formed
  3. filtrationwas filtered off
  4. washwashed with 50 ml of acetic acid
  5. customdried in air
  6. additionThen, this white solid was added to a solution of 100 g of potassium hydroxide in 400 ml of water
  7. stirringThis mixture was stirred for 30 min
  8. extractionThe crude product was extracted with 3×100 ml of dichloromethane
  9. extractionThe combined extract
  10. dry with materialwas dried over Na2SO4
  11. customevaporated to dryness
  12. distillationFractional distillation
  13. customgave a yellowish liquid, bp 83-85° C./1 mm Hg

출처 및 근거

ORD 기록
ord-285bd4f98d6243c282fb095cbe191fbb
출처 데이터셋
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07868197B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트