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

Potassium Carbonate → 1-Ethynyl-4-iodobenzene

HRID 18349
노트
인쇄 미리보기

반응식

HRID 18349 반응식
[I:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]#[C:9][Si](C)(C)C)=[CH:4][CH:3]=1.C([O-])([O-])=O.[K+].[K+]>CO>[C:8]([C:5]1[CH:6]=[CH:7][C:2]([I:1])=[CH:3][CH:4]=1)#[CH:9]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 11430Potassium CarbonateHCID 11808725(4-Iodophenylethynyl)trimethylsilane

생성물 1

HCID 121608331-Ethynyl-4-iodobenzene수율 64.8%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a solution of ((4-iodophenyl)ethynyl)trimethylsilane (5) (2.07 g, 6.23 mmol) in methanol (40 mL) was added K2CO3 (8.0 g, 57.9 mmol) and the reaction was allowed to stir for 48 hours. The volatiles were then removed in vacuo and the residue partitioned between ethyl acetate and H2O. The layers were separated and the aqueous phase re-extracted with ethyl acetate (2×). The combined organic layers were washed (H2O, brine), dried (Na2SO4), and filtered. The solvent was removed in vacuo and the residue was crystallized from hexane at −20° C. (in 2 crops) to give 1-ethynyl-4-iodobenzene (6) as a colorless solid (0.92 g, 64%). 1H NMR (400 MHz, DMSO-d6) δ 7.66 (app d, J=8.6 Hz, 2H), 7.20 (app d, J=8.5 Hz, 2H), 1.54 (s, 1H).

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

후처리

  1. customThe volatiles were then removed in vacuo
  2. customthe residue partitioned between ethyl acetate and H2O
  3. customThe layers were separated
  4. extractionthe aqueous phase re-extracted with ethyl acetate (2×)
  5. washThe combined organic layers were washed (H2O, brine)
  6. dry with materialdried (Na2SO4)
  7. filtrationfiltered
  8. customThe solvent was removed in vacuo
  9. customthe residue was crystallized from hexane at −20° C. (in 2 crops)

출처 및 근거

ORD 기록
ord-b4dda8d4d4954a57bf5cb0599e52ff3b
출처 데이터셋
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07741347B2

반응 노트

불러오는 중…