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

Sodium Carbonate → 2'-(2,4,6-Trimethoxybenzylthio)biphenyl-3-ol

HRID 1987476
노트
인쇄 미리보기

반응식

HRID 1987476 반응식
[CH3:1][O:2][C:3]1[CH:19]=[C:18]([O:20][CH3:21])[CH:17]=[C:16]([O:22][CH3:23])[C:4]=1[CH2:5][S:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1B(O)O.I[C:25]1[CH:26]=[C:27]([OH:31])[CH:28]=[CH:29][CH:30]=1.C([O-])([O-])=O.[Na+].[Na+]>[Pd].C1(C)C=CC=CC=1>[CH3:1][O:2][C:3]1[CH:19]=[C:18]([O:20][CH3:21])[CH:17]=[C:16]([O:22][CH3:23])[C:4]=1[CH2:5][S:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[C:25]1[CH:30]=[CH:29][CH:28]=[C:27]([OH:31])[CH:26]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 10340Sodium CarbonateHCID 122723-IodophenolHCID 686436172-(2,4,6-Trimethoxybenzylthio)phenylboronic acid

생성물 1

HCID 668706052'-(2,4,6-Trimethoxybenzylthio)biphenyl-3-ol수율 79%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 1140
Toluene
용매

실험 절차

To a mixture of 1.05 g 2-(2,4,6-trimethoxybenzylthio)phenylboronic acid (3.14 mmol), 1.07 g 3-iodophenol (4.9 mmol) and 0.195 g Pd catalyst was added 40 ml toluene followed by 15 ml 2M Na2CO3. The mixture was refluxed under nitrogen overnight. The mixture was extracted with ethyl acetate. The organic was washed with water, brine, dried over magnesium sulfate, and concentrated. The residue was purified by silica flash chromatography (hexane:ethyl acetate 80:20) to afford 0.948 g product (2.48 mmol, 79% yield).

후처리

  1. temperatureThe mixture was refluxed under nitrogen overnight
  2. extractionThe mixture was extracted with ethyl acetate
  3. washThe organic was washed with water, brine
  4. dry with materialdried over magnesium sulfate
  5. concentrationconcentrated
  6. customThe residue was purified by silica flash chromatography (hexane:ethyl acetate 80:20)

출처 및 근거

ORD 기록
ord-64398d0dc5114e009aa6aabb0854497d
출처 데이터셋
uspto-grants-2009_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07550505B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트