1620-30-0Relevant articles and documents
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Mislow
, p. 2559 (1947)
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Vittimberga et al.
, p. 4397 (1975)
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Preparation method of alpha, alpha-diphenyl-4-piperidine methanol
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Paragraph 0028-0030; 0037-0039; 0046-0048; 0055-0057, (2021/05/01)
The invention discloses a preparation method of alpha, alpha-diphenyl-4-piperidine methanol, which comprises the following steps of by using benzophenone and 4-cyanopyridine as raw materials, carrying out free radical coupling reaction under the action of alkali metal to obtain alpha, alpha-diphenyl-4-piperidine methanol, reacting the obtained alpha, alpha-diphenyl-4-pyridine methanol with a benzylation reagent to generate N-benzyl-alpha, alpha-diphenyl-4-pyridine methanol, carrying out hydroboration reduction on the N-benzyl-alpha, alpha-diphenyl-4-pyridine methanol to obtain (1-benzyl-1, 2, 3, 6-tetrahydropyridine-4-yl)benzhydrol, ane enabling (1-benzyl-1, 2, 3, 6-tetrahydropyridine-4-yl)benzhydrol to be subjected to catalytic hydrogenation and debenzylation protection to obtain alpha, alpha-diphenyl-4-piperidine methanol. The method has the advantages of cheap and accessible raw materials, high reaction yield and high controllability, and is suitable for industrial production requirements.
Preparation method of diphenyl(4-pyridyl)methanol
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Paragraph 0010, (2019/10/02)
The invention relates to a preparation method of diphenyl(4-pyridyl)methanol. According to the method, benzophenone and 4-cyanopyridine are taken as raw materials to carrying out a one-step reaction to prepare the diphenyl(4-pyridyl)methanol. The preparation method is simple in process, low in cost, high in yield and high in controllability, and is suitable for industrial production.