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

4-Hydroxybiphenyl → methyl (biphenyl-4-yloxy)acetate

HRID 1070391
노트
인쇄 미리보기

반응식

HRID 1070391 반응식
[C:1]1([C:7]2[CH:12]=[CH:11][C:10]([OH:13])=[CH:9][CH:8]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.Br[CH2:15][C:16]([O:18][CH3:19])=[O:17].C(=O)([O-])[O-].[Cs+].[Cs+]>CC(C)=O>[CH3:19][O:18][C:16](=[O:17])[CH2:15][O:13][C:10]1[CH:9]=[CH:8][C:7]([C:1]2[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=2)=[CH:12][CH:11]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 71034-HydroxybiphenylHCID 10796Cesium carbonateHCID 60984Methyl bromoacetate

생성물 1

HCID 2791909methyl (biphenyl-4-yloxy)acetate수율 95%

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

To a solution of 4-phenyl phenol (5.00 g, 29.38 mmol) in acetone (100 mL) was added at room temperature, methyl bromoacetate (2.92 mL, 30.84 mmol) and cesium carbonate (14.36 g, 44.06 mmol). The mixture was stirred at room temperature for 5 h. The white precipitate was filtered and the filtrate was concentrated to dryness. Purification by flash chromatography (Hex:EtOAc/7:3) gave 6.76 g of (biphenyl-4-yloxy)-acetic acid methyl ester as a white solid.

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

후처리

  1. filtrationThe white precipitate was filtered
  2. concentrationthe filtrate was concentrated to dryness
  3. customPurification by flash chromatography (Hex:EtOAc/7:3)

출처 및 근거

ORD 기록
ord-f021c79da94f413eb5daffeff73a157b
출처 데이터셋
uspto-grants-2005_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06903086B2

반응 노트

불러오는 중…