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

Potassium Carbonate → 1-Bromo-3-iodo-5-(4-methoxy-benzyloxy)-benzene

HRID 1784830
노트
인쇄 미리보기

반응식

HRID 1784830 반응식
[Br:1][C:2]1[CH:3]=[C:4]([OH:9])[CH:5]=[C:6]([I:8])[CH:7]=1.C(=O)([O-])[O-].[K+].[K+].[CH3:16][O:17][C:18]1[CH:25]=[CH:24][C:21]([CH2:22]Cl)=[CH:20][CH:19]=1>CN(C=O)C.C(OC)(C)(C)C.O.COC1C=CC(CCl)=CC=1>[Br:1][C:2]1[CH:3]=[C:4]([O:9][CH2:22][C:21]2[CH:24]=[CH:25][C:18]([O:17][CH3:16])=[CH:19][CH:20]=2)[CH:5]=[C:6]([I:8])[CH:7]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 3

HCID 11430Potassium CarbonateHCID 699934-Methyloxybenzyl chlorideHCID 226301823-Bromo-5-iodophenol

생성물 1

HCID 509940261-Bromo-3-iodo-5-(4-methoxy-benzyloxy)-benzene수율 77.8%

시약·촉매·용매 4

HCID 699934-Methyloxybenzyl chloride촉매HCID 962Water
용매
HCID 6228Dimethylformamide용매
HCID 15413tert-Butyl methyl ether용매

반응 조건

온도
0 °C

실험 절차

3-Bromo-5-iodo-phenol (8.48 g, 28.37 mmol) was dissolved in DMF (50 mL) under dry argon and cooled to 0° C. Then potassium carbonate (3.92 g, 28.37 mmol) was added, followed by drop wise addition of 4-methoxybenzyl chloride (3.7 mL, 27.0 mmol). The mixture was slowly warmed to room temperature and stirred for 20 h. Additional 4-methoxybenzyl chloride (0.19 mL, 1.4 mmol) was added and the mixture was stirred for additional 24 h at room temperature. The reaction mixture was diluted with tert-butylmethyl ether (300 mL) and water (150 mL). The layers were separated and the aqueous one extracted with tert-butylmethyl ether (2×150 mL). The combined organics were washed with water and brine (150 mL), dried (Na2SO4) and concentrated to give the crude product which was purified by flash chromatography on silica gel (330 g, AcOEt/heptane 1:9). 1-Bromo-3-iodo-5-(4-methoxy-benzyloxy)-benzene (8.80 g, 59%, purity 80%, HPLC 220 nm) was obtained as a yellow oil.

후처리

  1. temperatureThe mixture was slowly warmed to room temperature
  2. stirringthe mixture was stirred for additional 24 h at room temperature
  3. customThe layers were separated
  4. extractionthe aqueous one extracted with tert-butylmethyl ether (2×150 mL)
  5. washThe combined organics were washed with water and brine (150 mL)
  6. dry with materialdried (Na2SO4)
  7. concentrationconcentrated
  8. customto give the crude product which
  9. customwas purified by flash chromatography on silica gel (330 g, AcOEt/heptane 1:9)

출처 및 근거

ORD 기록
ord-c5c30b34a447446bb1f71cc9561ce8c5
출처 데이터셋
uspto-grants-2009_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07504401B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트