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HRID 1531612作成日:2026年10月27日

Tetrahydrofuran → Methyl Myristate

https://huagongshe.com/reaction/1531612

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物TriethylamineHCID 8471—
反応物Myristoyl chlorideHCID 66986—
反応物3,3-Bis(hydroxymethyl)oxetaneHCID 529229—
生成物Methyl MyristateHCID 3128474%

反応条件

温度0 °C

反応手順

Oxetane 2 (5 g, 41 mmol) was dried in vacuo at 100° C. for 1 h and then dissolved in THF (120 mL). To the solution at room temperature was added freshly distilled triethylamine (10 mL, 72 mmol) and N,N-(dimethylamino)pyridine (400 mg, 3.3 mmol) and the reaction was cooled to 0° C. Myristoyl chloride (8.9 mL, 33 mmol) was added via cannula to the reaction mixture, and the resulting yellowish solution was stirred at 0° C. for 4 h and then warmed to room temperature and stirred an additional 4 h. The reaction was quenched by addition of diethyl ether and washing with sat'd aq. NaHCO3, followed by washing with brine. The organic layer was separated and dried (Na2SO4). The solvents were removed by rotary evaporation, and the crude product was purified by silica gel column chromatography to yield 8 g (74%) of the ester 3 as white powder.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06200599B1
出典データセットuspto-grants-2001_03
ORD IDord-7aa3d9d46bf042f4823b7431f3d92986
出典メモuspto-grants-2001_03