(2R,3R,4R)-4-[2-(5-benzyloxypyridyl)]-2-hydroxy-3-methyl-butano-4-lactone

Base Information

Chemical Name:(2R,3R,4R)-4-[2-(5-benzyloxypyridyl)]-2-hydroxy-3-methyl-butano-4-lactone
CAS No.:909913-32-2
Molecular Formula:C₁₇H₁₇NO₄
Molecular Weight:299.326
Hs Code.:

Synonyms:(2R,3R,4R)-4-[2-(5-benzyloxypyridyl)]-2-hydroxy-3-methyl-butano-4-lactone

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (2R,3R,4R)-4-[2-(5-benzyloxypyridyl)]-2-hydroxy-3-methyl-butano-4-lactone

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Technology Process of (2R,3R,4R)-4-[2-(5-benzyloxypyridyl)]-2-hydroxy-3-methyl-butano-4-lactone

There total 5 articles about (2R,3R,4R)-4-[2-(5-benzyloxypyridyl)]-2-hydroxy-3-methyl-butano-4-lactone which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 74.0%

: (3R,4R)-4-(5-Benzyloxy-pyridin-2-yl)-4-(tert-butyl-dimethyl-silanyloxy)-2-hydroxy-3-methyl-butyric acid methyl ester

: (2S,3R,4R)-4-[2-(5-benzyloxypyridyl)]-2-hydroxy-3-methyl-butano-4-lactone

: 909913-32-2
(2R,3R,4R)-4-[2-(5-benzyloxypyridyl)]-2-hydroxy-3-methyl-butano-4-lactone

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 20 ℃; for 3h;
DOI:10.1016/j.tetasy.2006.06.010

Reference yield:

: 909913-42-4
(2R,3R)-1-acetoxy-3-[2-(5-benzyloxypyridyl)]-2-methyl-3-propanol

: 909913-32-2
(2R,3R,4R)-4-[2-(5-benzyloxypyridyl)]-2-hydroxy-3-methyl-butano-4-lactone

Guidance literature:: Multi-step reaction with 5 steps

1.1: 97 percent / imidazole / dimethylformamide / 12 h / 20 °C

2.1: 92 percent / potassium carbonate / methanol / 2 h / 20 °C

3.1: 42 percent / PCC / CH₂Cl₂ / 10 h / 20 °C

4.1: n-BuLi / tetrahydrofuran; hexane / 1.33 h / -78 - -20 °C

4.2: tetrahydrofuran; hexane / 4 h / -78 - 0 °C

4.3: 72 percent / HgCl₂; HgO / H₂O / 4 h / 20 °C

5.1: 74 percent / tetrabutylammonium fluoride / tetrahydrofuran / 3 h / 20 °C

With 1H-imidazole; n-butyllithium; tetrabutyl ammonium fluoride; potassium carbonate; pyridinium chlorochromate; In tetrahydrofuran; methanol; hexane; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.tetasy.2006.06.010

Reference yield:

: 909913-30-0
(2S,3R)-3-[2-(5-benzyloxypyridyl)]-3-tert-butyldimethylsilyloxy-2-methylpropanal

: 909913-32-2
(2R,3R,4R)-4-[2-(5-benzyloxypyridyl)]-2-hydroxy-3-methyl-butano-4-lactone

Guidance literature:: Multi-step reaction with 2 steps

1.1: n-BuLi / tetrahydrofuran; hexane / 1.33 h / -78 - -20 °C

1.2: tetrahydrofuran; hexane / 4 h / -78 - 0 °C

1.3: 72 percent / HgCl₂; HgO / H₂O / 4 h / 20 °C

2.1: 74 percent / tetrabutylammonium fluoride / tetrahydrofuran / 3 h / 20 °C

With n-butyllithium; tetrabutyl ammonium fluoride; In tetrahydrofuran; hexane;
DOI:10.1016/j.tetasy.2006.06.010