2,3-Dimethoxy-1,3-butadiene → 3,4-Dimethoxyselenophene

HRID 70756

반응식

HRID 70756 반응식
[CH3:1][O:2][C:3]([C:5]([O:7][CH3:8])=[CH2:6])=[CH2:4].CC(O[Na])=O.C(=O)=O.CC(C)=O.[Se:21](Cl)Cl>CCCCCC>[CH3:1][O:2][C:3]1[C:5]([O:7][CH3:8])=[CH:6][Se:21][CH:4]=1

참가 물질

6

반응 조건

온도
-78 °C

실험 절차

To a well stirred solution of 2,3-dimethoxy-1,3-butadiene (1.47 g, 12.9 mmol, (11)) and CH3COONa (2.64 g, 32.25 mmol) in dry hexane (80 mL) at −78° C. (dry ice/acetone bath), under an inert atmosphere, was added a solution of freshly prepared SeCl2 in hexane over a period of 15 min. The resulting yellowish solution was further stirred for 1 h at −78° C. and then removed from the cooling bath and the reaction mixture was brought to room temperature over a period of 2 h and further stirred for 5 h. The reaction mixture was filtered through neutral alumina and washed with hexane. The residue was concentrated to give brown yellow oil. The crude product was purified by flash column chromatography on TLC grade silica gel (Hexane:Ethyl acetate—95:5) to provide DMOS (0.85 g, 35%, (12)) as a white crystalline solid. mp. 43-45° C.

후처리

  1. customremoved from the cooling bath
  2. waitthe reaction mixture was brought to room temperature over a period of 2 h
  3. stirringfurther stirred for 5 h
  4. filtrationThe reaction mixture was filtered through neutral alumina
  5. washwashed with hexane
  6. concentrationThe residue was concentrated
  7. customto give brown yellow oil
  8. customThe crude product was purified by flash column chromatography on TLC grade silica gel (Hexane:Ethyl acetate—95:5)

출처 및 근거

ORD 기록
ord-18f9441165df4406b6d2489b4d5df025
출처 데이터셋
uspto-grants-2014_09
특허 번호
US08822635B2

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