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HRID 20053作成日:2026年10月24日

Water → 3-(Benzyloxy)cyclobutan-1-one

https://huagongshe.com/ja/reaction/20053

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物(((1,3-Dibromopropan-2-yl)oxy)methyl)benzeneHCID 561824—
反応物3-(Benzyloxy)cyclobutanone Methylsulfinyl(methylthio)methaneHCID 86614138—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物3-(Benzyloxy)cyclobutan-1-oneHCID 14932787—

反応条件

温度-20 °C

反応手順

3-(Benzyloxy)cyclobutanone Methylsulfinyl(methylthio)methane (13 ml, 125 mmol) was dissolved in 250 ml THF and cooled to −20° C. n-Butyllithium (50 ml, 125 mmol) was added and the mixture was stirred for 3 h at −20° C. The mixture was cooled down to −78° C. and a solution of 1-((1,3-dibromopropan-2-yloxy)methyl)benzene (16.000 g, 52 mmol) was added. The reaction was stirred over night and allowed to warm up to RT. It was stirred for an additional 6h at RT, hydrolyzed with water and extracted with EtOAc. The combined organic extracts were evaporated, dissolved in ether (50 ml) and treated with conc. HCl (10 ml) for 30 min at reflux. The mixture was neutralized with NaOH (10M) and extracted with EtOAc. The combined organic extracts were dried over MgSO4 and evaporated. Glass col. Chrom. (10-50% EtOAc in Hex) gave 3-(benzyloxy)cyclobutanone as a yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07745484B2
出典データセットuspto-grants-2010_06
ORD IDord-209392541b7d4708aa42d3647a0d987d
出典メモuspto-grants-2010_06