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HRID 5627作成日:2026年10月25日

3,4-dihydro-2H-pyran → rac-(2RS,3RS,5SR)-5-benzyloxy-2-hexyl-3-hydroxy-decanoic acid

https://huagongshe.com/reaction/5627

反応式

関与物質

役割名称HCID仕込み量
反応物3,4-dihydro-2H-pyranHCID 8080—
反応物Sodium HydroxideHCID 14798—
反応物PyridiniumHCID 4989215—
反応物3-Hexyl-4-hydroxy-6-undecyl-tetrahydropyran-2-oneHCID 10665857—
溶媒tert-Butyl methyl etherHCID 15413—
生成物rac-(2RS,3RS,5SR)-5-benzyloxy-2-hexyl-3-hydroxy-decanoic acidHCID 20084763—

反応手順

177.3 mg of rac-(2RS,3RS,5SR)-2-hexyl-3-hydroxy-5-undecyl-δ-valerolactone (Example 1c)), 750 ml of TBME, 86.7 g of 97% 3,4-dihydro-2H-pyran and 0.314 g of pyridinium p-toluenesulphone were stirred at 50° under argon for 20 hours. 500 ml of 2N sodium hydroxide solution were added to the reaction solution. After stirring at 50° for 2.5 hours the aqueous phase was separated and the organic phase was washed with 500 ml of 10% sodium chloride solution. salt slurry was cooled, treated under argon in succession with 152.7 g of benzyl bromide and 99.1 g of Na t-butylate and stirred at room temperature for 24 hours. After adding 750 ml of 2N hydrochloric acid and stirring at 50° for 22 hours the mixture was cooled, the aqueous phase was separated and the organic phase was washed with sodium chloride solution, dried and filtered. After evaporation of the solvent there were obtained 349.8 g of rac-(2RS,3RS,5SR)-5-benzyloxy-2-hexyl-3-hydroxy-decanoic acid (the product of Examples 1g and 12c)).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05245056
出典データセットuspto-grants-1993_09
ORD IDord-1e30286531164f3e818011ff3a8385c4
出典メモuspto-grants-1993_09