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Pyridine → 1-benzyl-1H-tetrazole-5-carbonyl chloride

HRID 325727
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HRID 325727 반응식
[CH2:1]([N:8]1[C:12]([C:13]([O-:15])=O)=[N:11][N:10]=[N:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[K+].N1C=CC=CC=1.C(Cl)(=O)C([Cl:26])=O>C1(C)C=CC=CC=1>[CH2:1]([N:8]1[C:12]([C:13]([Cl:26])=[O:15])=[N:11][N:10]=[N:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 1049PyridineHCID 65578Oxalyl chlorideHCID 23688251Potassium 1-Benzyl-1H-tetrazole-5-carboxylate

생성물 1

HCID 204638761-benzyl-1H-tetrazole-5-carbonyl chloride

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

A stirred mixture of potassium 1-benzyl-1H-tetrazole-5-carboxylate (3.6 g; prepared as described in the specification of Belgian Pat. No. 845612), dry pyridine (0.75 ml) and dry toluene (65 ml) was cooled to 5° C. and treated with oxalyl chloride (12.5 ml). Stirring was maintained and the temperature was allowed to rise to 15° C. during a period of 2 hours. The mixture was filtered and the residue was washed with dry toluene. Evaporation of the combined toluene filtrate and washings, under diminished pressure, gave crude 1-benzyl-1H-tetrazole-5-carbonyl chloride in the form of an oil, which was used without further purification.

후처리

  1. customprepared
  2. temperaturewas maintained
  3. filtrationThe mixture was filtered
  4. washthe residue was washed with dry toluene
  5. customEvaporation of the combined toluene filtrate and washings

출처 및 근거

ORD 기록
ord-f1bee3e5b52a45299e62e87f2db85a7d
출처 데이터셋
uspto-grants-1984_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04442115

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