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

((2-Bromoethyl)thio)benzene → 2-[2-(phenylthio)ethyl]-1H-isoindole-1,3(2H)-dione

HRID 2107032
노트
인쇄 미리보기

반응식

HRID 2107032 반응식
[C:1]1(=[O:11])[NH:5][C:4](=[O:6])[C:3]2=[CH:7][CH:8]=[CH:9][CH:10]=[C:2]12.[K].Br[CH2:14][CH2:15][S:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1>CN(C=O)C>[C:17]1([S:16][CH2:15][CH2:14][N:5]2[C:1](=[O:11])[C:2]3[C:3](=[CH:7][CH:8]=[CH:9][CH:10]=3)[C:4]2=[O:6])[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 78553((2-Bromoethyl)thio)benzeneHCID 24194345Phthalimide potassium salt

생성물 1

HCID 9344532-[2-(phenylthio)ethyl]-1H-isoindole-1,3(2H)-dione수율 69.2%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
90 °C

실험 절차

Potassium phthalimide (5.43 g, 25 mmol) was added to a DMF (50 ml) solution of [(2-bromoethyl)thio]benzene (5,43 g, 25 mmol) and this stirred mixture under N2 was heated at 90° C. for 2 h. After cooling to room temperature, the reaction was filtered. The solvent was stripped from the filtrate under reduced pressure. The residue, dissolved in CH2Cl2 (100 ml), was filtered, concentrated, and flash chromotographed on a 4 inch column eluting with 1 to 6% EtOAc/toluene to produce 4.9 g of the title product.

후처리

  1. temperatureAfter cooling to room temperature
  2. filtrationthe reaction was filtered
  3. dissolutionThe residue, dissolved in CH2Cl2 (100 ml)
  4. filtrationwas filtered
  5. concentrationconcentrated
  6. washeluting with 1 to 6% EtOAc/toluene

출처 및 근거

ORD 기록
ord-188ddf43ee3f40e19d7e862ad8b3ebb9
출처 데이터셋
uspto-grants-1990_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04933325

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트