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HRID 1384999作成日:2026年10月25日

Hydrochloric Acid → 3,4-dibenzyloxy-5-(2-hydroxyethyl)-2(5H)-furanone

https://huagongshe.com/reaction/1384999

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Benzyl BromideHCID 7498—
反応物DiisopropylethylamineHCID 81531—
反応物3-benzyloxy-4-hydroxy-5-(2-hydroxyethyl)-2(5H)-furanoneHCID 54723596—
溶媒TetrahydrofuranHCID 8028—
生成物3,4-dibenzyloxy-5-(2-hydroxyethyl)-2(5H)-furanoneHCID 2118410660%

反応手順

A mixture of 1.25 g (5 mmol) of 3-benzyloxy-4-hydroxy-5-(2-hydroxyethyl)-2(5H)-furanone, 15 mL of THF, 871 μL (5.0 mmol) of diisopropylethylamine and 631 μL (5.2 mmol) of benzyl bromide were combined under argon. The reaction mixture was warmed to reflux for 5 hours, and upon cooling, a suspension formed which was poured into 50 mL of 5% aqueous HCl solution and extracted with 100 mL of ether. The ether fraction was separated and sequentially washed with 30 mL of 5% aqueous HCl, 30 mL of H2O, 30 mL of saturated NaHCO3 solution, 30 mL of H2O, 30 mL of brine, dried (MgSO4) and concentrated to a colorless oil. Purification over silica gel using EtOAc/hexanes (2/3) provided 3,4-dibenzyloxy-5-(2-hydroxyethyl)-2(5H)-furanone as a faint pink colored oil (1.0 g, 60% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06262073B1
出典データセットuspto-grants-2001_07
ORD IDord-cb7ac1c9ba61482b871363cbb05890b1
出典メモuspto-grants-2001_07