Diethyl Ether → 3-Benzyloxy-2,2-dimethylpropanal

HRID 1284844

반응식

HRID 1284844 반응식
[Cr](O[Cr]([O-])(=O)=O)([O-])(=O)=O.[NH+]1C=CC=CC=1.[NH+]1C=CC=CC=1.[CH3:22][C:23]([CH3:35])([CH2:26][O:27][CH2:28][C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1)[CH2:24][OH:25].C(OCC)C>C(Cl)Cl>[CH3:22][C:23]([CH3:35])([CH2:26][O:27][CH2:28][C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1)[CH:24]=[O:25]

참가 물질

5

실험 절차

In a dry three-neck flask equipped with a mechanical stirrer and an addition funnel was placed 78.8 g (0.21 moles) of pyridinium dichromate, Aldrich Chemical, see Tetrahedron Lett., 399 (1979), ibid., 731, (1980) and 200 ml of dry CH2Cl2. The mixture was vigorously stirred and a solution of 26.8 g (0.138 mole) of 2,2-dimethyl-3-(phenylmethoxy)propanol, the product of Example 1a, in 50 ml of CH2Cl2 was added in one portion. The reaction was followed by gas liquid chromatography (GC) and required four days stirring at room temperature. The black brown reaction mixture was poured into 200 ml ethyl ether and the mixture was filtered through a dry silica gel column to obtain a colorless solution. Removal of solvent gave a residue which was distilled through a vigreux column to obtain the title compound, a colorless liquid, bp 72°-75°/0.02 mmHg.

후처리

  1. customIn a dry three-neck flask equipped with a mechanical stirrer and an addition funnel
  2. stirringrequired four days stirring at room temperature
  3. filtrationthe mixture was filtered through a dry silica gel column
  4. customto obtain a colorless solution
  5. customRemoval of solvent
  6. customgave a residue which
  7. distillationwas distilled through a vigreux column

출처 및 근거

ORD 기록
ord-045f2b032ca149ed984217cc3a49a998
출처 데이터셋
uspto-grants-1986_01
특허 번호
US04564476

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