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

3-Chloro-2-methyl-1-propene → N-[1-methyl-1-(3-chlorophenyl)ethyl]-2-methyl-2-propenylamine

HRID 1707232
노트
인쇄 미리보기

반응식

HRID 1707232 반응식
[CH3:1][C:2]([NH2:11])([C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([Cl:10])[CH:5]=1)[CH3:3].C(=O)([O-])[O-].[K+].[K+].Cl[CH2:19][C:20]([CH3:22])=[CH2:21]>CN(C)C=O>[CH3:3][C:2]([NH:11][CH2:21][C:20]([CH3:22])=[CH2:19])([C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([Cl:10])[CH:5]=1)[CH3:1]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 112413-Chloro-2-methyl-1-propeneHCID 11430Potassium CarbonateHCID 135695212-(3-Chlorophenyl)propan-2-amine

생성물 1

HCID 18962886N-[1-methyl-1-(3-chlorophenyl)ethyl]-2-methyl-2-propenylamine수율 75.8%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
85 °C

실험 절차

To 15 ml of N,N-dimethylformamide were added 2.6 g of 1-methyl-1-(3-chlorophenyl)ethylamine, 2.0 g of potassium carbonate and 2.1 g of 3-chloro-2-methylpropene, and the solution was then stirred at 85° C. for 1 hour. After potassium carbonate was removed by filtration, 100 ml of water were added, followed by extraction with toluene. The resultant extract was dried over anhydrous sodium sulfate, and then concentrated by an evaporator. Afterward, silica gel column chromatography was done to obtain 2.6 g of the desired amine.

후처리

  1. customAfter potassium carbonate was removed by filtration, 100 ml of water
  2. additionwere added
  3. extractionfollowed by extraction with toluene
  4. extractionThe resultant extract
  5. dry with materialwas dried over anhydrous sodium sulfate
  6. concentrationconcentrated by an evaporator

출처 및 근거

ORD 기록
ord-ab2f67676f654b0a8d6aeb85dda35479
출처 데이터셋
uspto-grants-1994_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05352655

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트