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Ethyl Acetate → 5-Bromo-2-(methylsulfinyl)pyridine

HRID 1046242
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반응식

HRID 1046242 반응식
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([S:8][CH3:9])=[N:6][CH:7]=1.C(OCC)(=[O:12])C>O.C(O)(=O)C>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([S:8]([CH3:9])=[O:12])=[N:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 8857Ethyl AcetateHCID 114242515-Bromo-2-(methylthio)pyridine

생성물 1

HCID 584853485-Bromo-2-(methylsulfinyl)pyridine

시약·촉매·용매 2

HCID 176Acetic Acid용매HCID 962Water용매2회

실험 절차

NalO4 (0.52 g) dissolved in water (0.5 mL) was added to a solution of 5-bromo-2-methylsulfanyl-pyridine (0.25 g) in acetic acid (3 mL) at room temperature. The resulting mixture was stirred at room temperature overnight. Then, water and ethyl acetate were added and the mixture was stirred for another 10 min. The organic phase was separated and washed with 10% aqueous Na2S2O3 solution, 10% aqueous K2CO3 solution, and brine. After drying (MgSO4), the solvent was evaporated to afford the title compound. Yield: 0.20 g (72% of theory); Mass spectrum (ESI+): m/z=220/222 (Br) [M+H]+.

후처리

  1. stirringthe mixture was stirred for another 10 min
  2. customThe organic phase was separated
  3. washwashed with 10% aqueous Na2S2O3 solution, 10% aqueous K2CO3 solution, and brine
  4. dry with materialAfter drying (MgSO4)
  5. customthe solvent was evaporated

출처 및 근거

ORD 기록
ord-deb7fa39ccb74c9b86cd34a40cf2f002
출처 데이터셋
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08569292B2

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