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

Iodoethane → HCID 15027468, 화합물

HRID 1090804
노트
인쇄 미리보기

반응식

HRID 1090804 반응식
[OH:1][C:2]([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1[OH:18])([CH2:9][CH2:10][CH3:11])[CH2:3][N:4]1[CH:8]=[CH:7][N:6]=[CH:5]1.[CH2:19](I)[CH3:20].[OH-].[Na+]>CN(C)C=O>[OH:1][C:2]([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1[O:18][CH2:19][CH3:20])([CH2:9][CH2:10][CH3:11])[CH2:3][N:4]1[CH:8]=[CH:7][N:6]=[CH:5]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6340IodoethaneHCID 14798Sodium HydroxideHCID 15027467HCID 15027467, 화합물2회

생성물 1

HCID 15027468HCID 15027468, 화합물수율 58.1%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

34 mg of 1-[2-hydroxy-2-(2-hydroxyphenyl)pentyl]imidazole (Compound 18) was dissolved into 10 ml of dimethylformamide, and 33 mg of ethyl iodide and 10 mg of sodium hydroxide was added to this solution. The mixture was stirred at room temperature for 20 hours. The reaction mixture, after being charged into ice water, was subjected to extraction with ether. The ether layer was then washed with water, followed by drying over anhydrous magnesium sulfate. The extract thus obtained was purified by means of silica gel column chromatography (eluent: methylene chloride) to produce 22 mg of the title compound at a yield of 58%.

후처리

  1. additionwas added to this solution
  2. extractionwas subjected to extraction with ether
  3. washThe ether layer was then washed with water
  4. dry with materialby drying over anhydrous magnesium sulfate
  5. extractionThe extract thus
  6. customobtained
  7. customwas purified by means of silica gel column chromatography (eluent: methylene chloride)

출처 및 근거

ORD 기록
ord-9d646430d3484bfc8bf378d752f01c99
출처 데이터셋
uspto-grants-1992_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05082948

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트