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HRID 19779作成日:2026年10月26日

Benzyl Chloride → 1-Benzyloxy-2-tert-butyl-4-methyl-benzene

https://huagongshe.com/reaction/19779

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl ChlorideHCID 7503—
反応物Potassium CarbonateHCID 11430—
反応物2-tert-Butyl-4-methylphenolHCID 17004—
溶媒DimethylformamideHCID 6228—
生成物1-Benzyloxy-2-tert-butyl-4-methyl-benzeneHCID 50886343—

反応手順

8 g of 2-tert-Butyl-4-methyl-phenol (49 mmol) and 16.36 g of potassium carbonate (58 mmol) were stirred in 120 ml DMF until a suspension was formed. 6.74 ml of benzylchloride were then added dropwise and the reaction mixture was stirred for 24 h at RT. After two hours heating at 60° C., the reaction mixture was cooled to RT, filtered off, diluted with ethyl acetate, and washed with water followed by brine. The organic phase was dried over magnesium sulphate, filtered off and concentrated under vacuo. The residue was purified by flash column chromatography (heptane/AcOEt 98/2) to give 8.647 g of a colorless liquid. MS (ISP) 255.3 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07745477B2
出典データセットuspto-grants-2010_06
ORD IDord-8cdae5bcb04442f4acfe2417bcb9c0c9
出典メモuspto-grants-2010_06