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Carbon Dioxide → 5,6-Dimethoxy-2-methylbenzotellurazole

HRID 543073
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인쇄 미리보기

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HRID 543073 반응식
[Cl-].[CH3:2][O:3][C:4]1[C:5]([O:14][CH3:15])=[CH:6][C:7]2[Te:11][C:10]([CH3:12])=[NH+:9][C:8]=2[CH:13]=1.C(=O)(O)[O-].[Na+].C(=O)=O>O>[CH3:2][O:3][C:4]1[C:5]([O:14][CH3:15])=[CH:6][C:7]2[Te:11][C:10]([CH3:12])=[N:9][C:8]=2[CH:13]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 280Carbon DioxideHCID 516892Sodium BicarbonateHCID 147455505,6-Dimethoxy-2-methylbenzotellurazolium chloride

생성물 1

HCID 139312085,6-Dimethoxy-2-methylbenzotellurazole수율 95.2%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

5,6-Dimethoxy-2-methylbenzotellurazolium chloride (Example 12) (10 g) was ground with an equal quantity of sodium bicarbonate and a little water in a mortar until evolution of carbon dioxide ceased. The product was collected by filtration, washed with water and dried in a vacuum to yield ≃8.5 g of colorless powder, m.p. 78°-80° C. Slow crystallization from cyclohexane yielded well defined prisms, m.p. 80°-83° C. The mass spectra and nuclear magnetic resonance spectra were in agreement with that expected for the structural formula.

후처리

  1. filtrationThe product was collected by filtration
  2. washwashed with water
  3. customdried in a vacuum

출처 및 근거

ORD 기록
ord-1732b05bec2c461cbd35758823a3ed53
출처 데이터셋
uspto-grants-1987_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04661438

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