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

Iodoethane → 2'-Ethoxyl-1,1'-biphenyl-2-ol

HRID 844591
노트
인쇄 미리보기

반응식

HRID 844591 반응식
[C:1]1([OH:14])[C:2]([C:7]2[C:8]([OH:13])=[CH:9][CH:10]=[CH:11][CH:12]=2)=[CH:3][CH:4]=[CH:5][CH:6]=1.C(=O)([O-])[O-].[K+].[K+].I[CH2:22][CH3:23]>CC(C)=O>[O:14]([C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[C:7]1[C:8]([OH:13])=[CH:9][CH:10]=[CH:11][CH:12]=1)[CH2:22][CH3:23]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6340IodoethaneHCID 11430Potassium CarbonateHCID 15731(1,1'-Biphenyl)-2,2'-diol

생성물 1

HCID 226138842'-Ethoxyl-1,1'-biphenyl-2-ol

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

2′-Ethoxyl-1,1′-biphenyl-2-ol was prepared by modifying the procedure reported in J. Org. Chem. 1981, 46, 4988. In 50 mL of acetone was added 10 g of 2,2′-biphenol and 9.4 g of potassium carbonate. After stirring at room temperature for one hour, a solution of iodoethane (9.2 g in 10 mL of acetone) was added slowly dropwise. The mixture was filtered, washed with acetone, and solvent removed by rotary evaporation. The residue was flashed chromatographed to give 5.1 g of the2′-ethoxyl-1,1′-biphenyl-2-ol as a colorless oil. 1H NMR (C6D6): 7.20 (m, 3H), 7.10 (m, 1H), 7.05 (m, 1H), 6.85 (m, 2H), 6.55 (m, 1H), 3.38 (q, 2H), 0.81 (t, 3H).

후처리

  1. filtrationThe mixture was filtered
  2. washwashed with acetone, and solvent
  3. customremoved by rotary evaporation
  4. customThe residue was flashed chromatographed

출처 및 근거

ORD 기록
ord-6e2e9ef1e87a416cb7b3c19e96d2e5b2
출처 데이터셋
uspto-grants-2002_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06380421B1

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트