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HRID 1962216作成日:2026年10月27日

Ethyl Acetate → Ethyl 3-oxo-3-(oxolan-3-yl)propanoate

https://huagongshe.com/reaction/1962216

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物Lithium HexamethyldisilazideHCID 2733832—
反応物Methyl oxolane-3-carboxylateHCID 10678263—
溶媒TetrahydrofuranHCID 8028—
生成物Ethyl 3-oxo-3-(oxolan-3-yl)propanoateHCID 2283188138.4%

反応手順

To a solution of lithium bis(trimethylsilyl)amide (1 M in hexanes; 100 mL) in THF (200 mL) at −78° C. was added dry ethyl acetate (10.8 g, 12 mL, 122.5 mmol) dropwise. After 30 min at −78° C., the mixture was treated with a solution of tetrahydro-furan-3-carboxylic acid methyl ester (6.0 g, 46.1 mmol) in THF (50 mL). After 4 h at −78° C., the reaction was quenched with satd. aq. NH4Cl, warmed to rt, and extracted with EtOAc (5×75 mL). The combined organic layers were washed with satd. aq. NaCl, dried, and concentrated to give a colorless oil. Chromatography on SiO2 (EtOAc/CH2Cl2) afforded the title compound (3.3 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08415366B2
出典データセットuspto-grants-2013_04
ORD IDord-acf1dd432b094e52b8a7ca7dac066c39
出典メモuspto-grants-2013_04