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

Dimethylamine → 4-Bromo-2-(dimethylaminomethyl)-1-fluorobenzene

HRID 1066841
노트
인쇄 미리보기

반응식

HRID 1066841 반응식
[F:1][C:2]1[CH:9]=[CH:8][C:7]([Br:10])=[CH:6][C:3]=1[CH2:4]Br.[CH3:11][NH:12][CH3:13]>CO>[CH3:11][N:12]([CH2:4][C:3]1[CH:6]=[C:7]([Br:10])[CH:8]=[CH:9][C:2]=1[F:1])[CH3:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 674DimethylamineHCID 135532954-Bromo-2-(bromomethyl)-1-fluorobenzene

생성물 1

HCID 211961754-Bromo-2-(dimethylaminomethyl)-1-fluorobenzene

시약·촉매·용매 1

HCID 887Methanol용매2회

실험 절차

In a 50 ml flask, under a nitrogen atmosphere, 2-fluoro-5-bromobenzyl bromide (1.264 g, 4.72 mmol) was dissolved in methanol (10 ml). Dimethylamine (8 M in H2O, 1.77 ml, 14.2 mmol) was added as a solution in methanol (5 ml), and the resulting mixture was stirred at ambient temperature for about two hours. The progress of the reaction was monitored by thin layer chromatography. The methanol was removed by evaporation. The residue was partitioned between 1 M potassium carbonate and diethyl ether. The aqueous fraction was back extracted with diethyl ether. The organic fractions were combined, washed with brine (7×) and dried over sodium sulfate. The solvents were removed in vacuo. The title intermediate was used without further purification.

후처리

  1. customThe methanol was removed by evaporation
  2. customThe residue was partitioned between 1 M potassium carbonate and diethyl ether
  3. extractionThe aqueous fraction was back extracted with diethyl ether
  4. washwashed with brine (7×)
  5. dry with materialdried over sodium sulfate
  6. customThe solvents were removed in vacuo
  7. customThe title intermediate was used without further purification

출처 및 근거

ORD 기록
ord-8d679847236e4b9daf1a1484f9bdf501
출처 데이터셋
uspto-grants-2001_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06245761B1

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트