Hydrogen Peroxide → 2-tert-Butyl-1-oxo-1lambda~5~-pyridinato

HRID 2225155노트

반응식

HRID 2225155 반응식
[C:1]([C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][N:6]=1)([CH3:4])([CH3:3])[CH3:2].[OH:11]O>CC(O)=O.C(Cl)Cl>[C:1]([C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][N+:6]=1[O-:11])([CH3:4])([CH3:3])[CH3:2]

참가 물질

5

반응물 2

HCID 784Hydrogen PeroxideHCID 1386302-tert-Butylpyridine

생성물 1

HCID 187150642-tert-Butyl-1-oxo-1lambda~5~-pyridinato수율 71.5%

시약·촉매·용매 2

HCID 176Acetic Acid용매HCID 6344Dichloromethane용매

실험 절차

Preparation C3, Step 1: 2-tert-butylpyridine (2.00 g, 14.8 mmol, 1 eq.) was dissolved in HOAc (10 mL) and 30% hydrogen peroxide (1.68 mL, 14.8 mmol, 1 eq.) at room temperature then the reaction was refluxed for 20 hours. The reaction was stripped to obtain an amber oil which was dissolved in methylene chloride (10 mL) then dried over sodium sulfate and stripped to obtain 2-tert-butylpyridine-N-oxide (1.60 g) as an amber oil. Yield=71.5%. LCMS detects (M+H)+=152.09.

후처리

  1. customto obtain an amber oil which
  2. dry with materialthen dried over sodium sulfate

출처 및 근거

ORD 기록
ord-4b1dd3f414b84937a21c00a0534e0dc5
출처 데이터셋
uspto-grants-2008_05
특허 번호
US07378409B2

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