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Sulfuric Acid → 1-tert-Butyl-5-(2-bromophenyl)-1H-tetrazole

HRID 1886062
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HRID 1886062 반응식
[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[NH:12][N:11]=[N:10][N:9]=1.[CH3:13][C:14](O)([CH3:16])[CH3:15].OS(O)(=O)=O>FC(F)(F)C(O)=O>[C:14]([N:9]1[C:8]([C:3]2[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=2[Br:1])=[N:12][N:11]=[N:10]1)([CH3:16])([CH3:15])[CH3:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 1118Sulfuric AcidHCID 6386tert-ButanolHCID 1784193735-(2-Bromophenyl)-1H-tetrazole

생성물 1

HCID 218408841-tert-Butyl-5-(2-bromophenyl)-1H-tetrazole수율 67.1%

시약·촉매·용매 1

HCID 6422Trifluoroacetic acid용매

실험 절차

To a solution of 5-(2-bromophenyl)-1H-tetrazole (7.9 g, 0.035 mol) in trifluoroacetic acid (35 mL) was added tBuOH (5.2 g, 0.070 mol) and H2SO4 (1.0 mL, 0.0175 mol). After 18 h, the solution was concentrated and the residue was taken up in EtOAc. The mixture was washed with water, 2.5N NaOH, water, dried (MgSO4), and concentrated. Purification by flash chromatography (20% EtOAc/hexane) gave 6.6 g (67%) of product as a pale yellow oil.

후처리

  1. concentrationthe solution was concentrated
  2. washThe mixture was washed with water, 2.5N NaOH, water
  3. dry with materialdried (MgSO4)
  4. concentrationconcentrated
  5. customPurification by flash chromatography (20% EtOAc/hexane)

출처 및 근거

ORD 기록
ord-f68114dee73a4de982dab59f03da1590
출처 데이터셋
uspto-grants-1992_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05149699

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