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HRID 227374作成日:2026年10月26日

Ethyl tetrahydropyran-4-ylacetate → 2-(Oxan-4-yl)ethan-1-ol

https://huagongshe.com/reaction/227374

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl tetrahydropyran-4-ylacetateHCID 2773412—
反応物Aluminium lithium hydrideHCID 21226445—
溶媒TetrahydrofuranHCID 8028—
生成物2-(Oxan-4-yl)ethan-1-olHCID 17750944—

反応手順

To 15 mL of tetrahydrofuran (THF) at 0° C. was added LiAlH4 (0.28 g, 7.3 mmol). This mixture was stirred for 10 min then the ethyl tetrahydropyran-4-yl-acetate (Combi-Blocks Inc., 0.50 g, 2.9 mmol) was added. The reaction was stirred for 5 min at 0° C. then was allowed to warm to ambient temperature and was stirred for 90 min. The reaction was quenched with excess NaHSO4.10H2O and was stirred for 60 min. The mixture was filtered through Celite. The filtrate was concentrated to give the title compound which was carried on without further purification. MS (DCI/NH3) m/z 131 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07560481B2
出典データセットuspto-grants-2009_07
ORD IDord-5976d4588e174b91ab708aed313d55d1
出典メモuspto-grants-2009_07