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Sodium Azide → 3-bromo-5-nitrophenyl-1-methyl-1H-tetrazole

HRID 1422392
ノート
印刷プレビュー

反応式

HRID 1422392 の反応式
[Br:1][C:2]1[CH:3]=[C:4]([CH:9]=[C:10]([N+:12]([O-:14])=[O:13])[CH:11]=1)[C:5]([NH:7][CH3:8])=O.S(OS(C(F)(F)F)(=O)=O)(C(F)(F)F)(=O)=O.[N-:30]=[N+:31]=[N-:32].[Na+].C([O-])(O)=O.[Na+]>C(Cl)Cl>[Br:1][C:2]1[CH:3]=[C:4]([C:5]2[N:7]([CH3:8])[N:32]=[N:31][N:30]=2)[CH:9]=[C:10]([N+:12]([O-:14])=[O:13])[CH:11]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 33557Sodium AzideHCID 67749Trifluoromethanesulfonic anhydrideHCID 516892Sodium BicarbonateHCID 222526863-Bromo-N-methyl-5-nitrobenzamide

生成物 1

HCID 222526903-bromo-5-nitrophenyl-1-methyl-1H-tetrazole収率 44.1%

試薬・触媒・溶媒 1

HCID 6344
Dichloromethane
溶媒

実験手順

To a solution of 3-bromo-N-methyl-5-nitro-benzamide (0.6 g) in DCM (15 ml) at −15° C. was added triflic anhydride (0.6 ml) and the reaction stirred for 30 min. Sodium azide (226 mg) was added and the reaction allowed to warm to room temperature and stirred further overnight. NaHCO3(aq) was added to neutralise the reaction and the mixture extracted into EtOAc. The organic layer was separated, dried and concentrated in vacuum and the residue purified by flash chromatography (9:1 to 2:8 cyclohexane:EtOAc) to give the title compound (290 mg). Rf=0.51 (3:2 cyclohexane:EtOAc).

後処理

  1. stirringstirred further overnight
  2. customthe reaction
  3. extractionthe mixture extracted into EtOAc
  4. customThe organic layer was separated
  5. customdried
  6. concentrationconcentrated in vacuum
  7. customthe residue purified by flash chromatography (9:1 to 2:8 cyclohexane:EtOAc)

出典と根拠

ORDレコード
ord-4d35fc24975a46cd8faf905fd7ed430b
出典データセット
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
USRE045323E1

反応ノート

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