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Methyl iodide → HCID 22402931, 화합물

HRID 259720
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HRID 259720 반응식
C[O-].[Na+].[CH3:4][C:5]1[NH:6][C:7]2[CH:13]=[C:12]([C:14]([O:16][CH3:17])=[O:15])[C:11]([C:18]([O:20][CH3:21])=[O:19])=[CH:10][C:8]=2[N:9]=1.IC.[C:24](=O)(O)[O-].[Na+]>CO.C(O)(=O)C>[CH3:24][N:9]1[C:8]2[CH:10]=[C:11]([C:18]([O:20][CH3:21])=[O:19])[C:12]([C:14]([O:16][CH3:17])=[O:15])=[CH:13][C:7]=2[N:6]=[C:5]1[CH3:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 6328Methyl iodideHCID 516892Sodium BicarbonateHCID 10942334Sodium MethoxideHCID 21827571HCID 21827571, 화합물

생성물 1

HCID 22402931HCID 22402931, 화합물수율 69.7%

시약·촉매·용매 2

HCID 176Acetic Acid용매
HCID 887
Methanol
용매

실험 절차

Sodium methoxide (1.96 g, 36.3 mmol) is added to a solution of dimethyl 2-methyl-5,6-benzimidazoledicarboxylate (8.50 g, 34.2 mmol) in methanol. The reaction mixture is stirred 0.5 hour at room temperature, treated with iodomethane (2.15 mL, 34.5 mmol) stirred overnight, acidified to pH 6 with acetic acid, treated with sodium bicarbonate to pH 8 and extracted with chloroform. The extracts are combined, dried (MgSO4) and concentrated in vacuo to yield the title product as a pink solid (6.25 g, 69.7%). A small portion is recrystallized from ethyl acetate to afford the title product as pink crystals, mp 147°-148° C.

후처리

  1. stirringstirred overnight
  2. extractionextracted with chloroform
  3. dry with materialdried (MgSO4)
  4. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-690ab6e5f2634c848bf7fcc5ebb43b55
출처 데이터셋
uspto-grants-1996_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05523279

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