Potassium Carbonate → 1-(benzyloxymethyl)-2H-tetrazole

HRID 1016179

반응식

HRID 1016179 반응식
[NH:1]1[CH:5]=[N:4][N:3]=[N:2]1.C(=O)([O-])[O-].[K+].[K+].Cl[CH2:13][O:14][CH2:15][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1>CN(C=O)C>[CH2:15]([O:14][CH2:13][N:2]1[N:3]=[N:4][CH:5]=[N:1]1)[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1.[CH2:15]([O:14][CH2:13][N:1]1[CH:5]=[N:4][NH:3][NH:2]1)[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1

참가 물질

6

실험 절차

A suspension of 1-H-tetrazole (2.0 g, 28.5 mmol) and potassium carbonate (5.9 g, 42.7 mmol) in DMF (30 mL) was treated with benzyl chloromethyl ether (5.36 g, 34.2 mmol), and the mixture was stirred for 4 hours. Analysis by LC/MS indicated that the reaction was not complete, so the reaction was treated with benzyl chloromethyl ether (0.5 g, 3.19 mmol) and stirred overnight. The mixture was filtered, and the filtrate was concentrated in-vacuo. The residue was diluted with diethyl ether (200 mL), washed 5× with water (50 mL), once with brine, dried over sodium sulfate, and concentrated in-vacuo. The residue was purified over a 6×20 mm silica gel column, eluting with 20% then 30% ethyl acetate/hexanes to yield the title compound (2.39 g, 44% yield), and 1-(benzyloxymethyl)-2H-tetrazole (2.56 g, 47% yield).

후처리

  1. stirringstirred overnight
  2. filtrationThe mixture was filtered
  3. concentrationthe filtrate was concentrated in-vacuo
  4. additionThe residue was diluted with diethyl ether (200 mL)
  5. washwashed 5× with water (50 mL)
  6. dry with materialonce with brine, dried over sodium sulfate
  7. concentrationconcentrated in-vacuo
  8. customThe residue was purified over a 6×20 mm silica gel column
  9. washeluting with 20%

출처 및 근거

ORD 기록
ord-9e3632809eb14d998e770946a3548e0d
출처 데이터셋
uspto-grants-2011_07
특허 번호
US07985861B2

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