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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Imidazole → 5-Ethenyl-2-methoxyphenol

HRID 2357423
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HRID 2357423 반응식
C(O)(=O)/[CH:2]=[CH:3]/[C:4]1[CH:12]=[CH:11][C:9]([OH:10])=[C:6]([O:7]C)[CH:5]=1.[C:15]([O-])([O-])=O.[K+].[K+].N1C=CN=C1>CN(C)C=O>[CH:3]([C:4]1[CH:5]=[C:6]([OH:7])[C:9]([O:10][CH3:15])=[CH:11][CH:12]=1)=[CH2:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 795ImidazoleHCID 11430Potassium CarbonateHCID 445858Ferulic Acid

생성물 1

HCID 104418575-Ethenyl-2-methoxyphenol수율 59%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

A mixture of Ferulic acid (0.0083 mol), K2CO3 (10%, 3 ml), imidazole (1 mL) and dimethylformamide (15 ml) were taken in a 250 ml Erlenmeyer flask fitted with a loose funnel at the top. The flask was shaken well and placed inside the microwave oven over an ice bath and irradiated for 30 minutes in parts. After completion of reaction, it was worked up and purified as in example V and provided sweet and pleasant smelling viscous liquid. 59% yield; (Spectral data as in example V)

후처리

  1. customfitted with a loose funnel at the top
  2. customplaced inside the microwave oven over an ice bath
  3. customirradiated for 30 minutes in parts
  4. customAfter completion of reaction, it
  5. custompurified as in example V
  6. customprovided sweet

출처 및 근거

ORD 기록
ord-21b7353b9fd14b59afa306d8c6c09164
출처 데이터셋
uspto-grants-2010_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07759527B2

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