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HRID 271840作成日:2026年10月27日

Tetrahydrofuran → 2-Phenethyl-cyclohexanone

https://huagongshe.com/reaction/271840

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物1-Chloro-2-phenylethaneHCID 231496—
反応物CID 53628100HCID 178418400—
生成物2-Phenethyl-cyclohexanoneHCID 231615—

反応条件

温度-78 °C

反応手順

s-BuLi (28.0 mL, 1.3 M) was added slowly to a solution of Compound 20b (7.0 g) in THF (50 mL) at −78° C. The mixture stirred for 1 hr at −78° C. and then (2-chloro-ethyl)-benzene Compound 20c (5.11 g, 36.4 mmol) in THF (10 mL) was added dropwise. The reaction mixture was stirred for 24 hrs while warming to r.t. The reaction was quenched with 1N HCl (5 mL), then diluted with water (100 mL) and EtOAc (500 mL). The organic layer was washed with brine, separated and dried with anhydrous sodium sulfate, then filtered and concentrated in vacuo to yield a crude product. Purification by flash chromatography (eluted with 10% EtOAc in Hexane) afforded 2-phenethyl-cyclohexanone Compound 20d (4.05 g, 20.0 mMol, 58%) as a yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07452997B2
出典データセットuspto-grants-2008_11
ORD IDord-5e24323ad1164353bd8e9c877b49b9ce
出典メモuspto-grants-2008_11