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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Imidazole → HCID 19045277, 화합물

HRID 1591200
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HRID 1591200 반응식
Cl[CH2:2][C:3]1[CH:4]=[CH:5][C:6]([OH:12])=[C:7]([C:9](=[O:11])[CH3:10])[CH:8]=1.CN(C)C=O.[Na].[NH:19]1[CH:23]=[CH:22][N:21]=[CH:20]1>>[C:9]([C:7]1[CH:8]=[C:3]([CH2:2][N:19]2[CH:23]=[CH:22][N:21]=[CH:20]2)[CH:4]=[CH:5][C:6]=1[OH:12])(=[O:11])[CH3:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 795ImidazoleHCID 225570132-Acetyl-4-chloromethyl phenolHCID 86746767Sodium dimethylformamide

생성물 1

HCID 19045277HCID 19045277, 화합물수율 33%

실험 절차

To a mixture of 5'-(chloromethyl)-2'-hydroxyacetophenone (1.85 g, 10.0 mmol), sodium dimethylformamide was added imidazole (0.75 g, 11.0 mmol). The mixture was stirred four hours and concentrated in vacuo. The residue was stirred under 50 mL ethanol, filtered, and the filtrate concentrated in vacuo to give a residue. The residue was stirred under 30 mL chloroform, filtered, and the filtrate concentrated in vacuo to give crude product. The crude product was purified by flash chromatography eluting with 5:95 methanol:chloroform to give a solid. The solid was recrystallized from n-butlychloride to give 0.71 g (33%) product as a yellow crystalline solid, mp 106°-107° C.

후처리

  1. concentrationconcentrated in vacuo
  2. stirringThe residue was stirred under 50 mL ethanol
  3. filtrationfiltered
  4. concentrationthe filtrate concentrated in vacuo
  5. customto give a residue
  6. stirringThe residue was stirred under 30 mL chloroform
  7. filtrationfiltered
  8. concentrationthe filtrate concentrated in vacuo
  9. customto give crude product
  10. customThe crude product was purified by flash chromatography
  11. washeluting with 5:95 methanol
  12. customchloroform to give a solid
  13. customThe solid was recrystallized from n-butlychloride

출처 및 근거

ORD 기록
ord-20b3fb84de804f90b4ef99bd61650cba
출처 데이터셋
uspto-grants-1993_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05206240

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