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HRID 1009160作成日:2026年10月27日

Water → 3-(Benzyloxy)cyclobutan-1-one

https://huagongshe.com/reaction/1009160

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Methyl (methylsulfinyl)methyl sulfideHCID 99129—
反応物(((1,3-Dibromopropan-2-yl)oxy)methyl)benzeneHCID 561824—
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

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 6 h 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US07973047B2
出典データセットuspto-grants-2011_07
ORD IDord-62640e8f36fa48219755166f11fe779e
出典メモuspto-grants-2011_07