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

Phosphorus tribromide → 5-(2-Bromoethyl)-2,3-dihydro-1-benzofuran

HRID 1463884
노트
인쇄 미리보기

반응식

HRID 1463884 반응식
P(Br)(Br)[Br:2].O[CH2:6][CH2:7][C:8]1[CH:9]=[CH:10][C:11]2[O:15][CH2:14][CH2:13][C:12]=2[CH:16]=1>C(Cl)(Cl)(Cl)Cl>[Br:2][CH2:6][CH2:7][C:8]1[CH:9]=[CH:10][C:11]2[O:15][CH2:14][CH2:13][C:12]=2[CH:16]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24614Phosphorus tribromideHCID 212240782-(2,3-Dihydro-1-benzofuran-5-yl)ethan-1-ol

생성물 1

HCID 218311605-(2-Bromoethyl)-2,3-dihydro-1-benzofuran

시약·촉매·용매 1

HCID 5943Carbon Tetrachloride용매

실험 절차

Phosphorus tribromide (0.37 g) was added to a solution of 5-(2-hydroxyethyl)-2,3-dihydrobenzofuran (0.612 g--see Preparation 19) in carbon tetrachloride (3 ml) and the mixture heated under reflux for 3 hours. On cooling to room temperature, the mixture was partitioned between 10% aqueous sodium carbonate (20 ml) and dichloromethane (20 ml). The layers were separated and the aqueous layer extracted with dichloromethane (3×10 ml). The combined dichloromethane extracts were dried (MgSO4) and concentrated in vacuo to give the title compound as an oil which crystallised on standing, yield 0.584 g, m.p. 60°-62°.

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

후처리

  1. temperaturethe mixture heated
  2. temperatureunder reflux for 3 hours
  3. customthe mixture was partitioned between 10% aqueous sodium carbonate (20 ml) and dichloromethane (20 ml)
  4. customThe layers were separated
  5. extractionthe aqueous layer extracted with dichloromethane (3×10 ml)
  6. dry with materialThe combined dichloromethane extracts were dried (MgSO4)
  7. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-ace066189e674b949d8bf920936785f5
출처 데이터셋
uspto-grants-1994_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05302595

반응 노트

불러오는 중…