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HRID 585564作成日:2026年10月25日

Tetrahydrofuran → Tert-butyl (5-oxotetrahydrofuran-3-yl)acetate

https://huagongshe.com/reaction/585564

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物2(5H)-FuranoneHCID 10341—
反応物tert-Butyl acetateHCID 10908—
反応物Lithium diisopropylamide mono(tetrahydrofuran)HCID 10997623—
溶媒WaterHCID 962—
生成物Tert-butyl (5-oxotetrahydrofuran-3-yl)acetateHCID 1364187472%

反応条件

温度-78 °C

反応手順

Tetrahydrofuran (50 mL) and Lithium diisopropylamide mono tetrahydrofuran complex (20 mL of 1.5 M in cyclohexane) was cooled in a dry ice/Isopropanol bath for 10 min. Tert-butyl acetate (3.5 mL 26 mmoles) was added via syringe and stirred at −78° C. for 30 min. 2(5H)-Furanone (1.59 g, 19 mmoles) was added dropwise and the reaction was stirred for 1 h at −78° C. The reaction was poured into water and extracted with ether 2×150 mL The ether extracts were combined and washed with water 100 mL then brine 3×100 mL, dried and the ether removed under reduced pressure to give 2.74 g of product (72%). MS (ESI+) for C10H16O4 m/z 223 (M+Na)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06933304B2
出典データセットuspto-grants-2005_08
ORD IDord-fc08a066caf44aa091c8db1dae39c476
出典メモuspto-grants-2005_08