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HRID 1879675作成日:2026年10月27日

Phenol, 3-(1,1-dimethylethyl)- → 2-[2-(3-Tert-butyl-phenoxy)-ethyl]-[1,3]dioxane

https://huagongshe.com/reaction/1879675

反応式

関与物質

役割名称HCID仕込み量
反応物Phenol, 3-(1,1-dimethylethyl)-HCID 11450—
反応物Sodium HydroxideHCID 14798—
反応物1,3-Dioxane, 2-(2-bromoethyl)-HCID 520656—
溶媒Acetic AcidHCID 176—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
生成物2-[2-(3-Tert-butyl-phenoxy)-ethyl]-[1,3]dioxaneHCID 59548552—

反応手順

Sodium hydroxide (3.46 g, 1.3 eq) was taken up in water (20 mL) and stirred for about 30 minutes. Then 3-tert-butyl phenol (10.0 g, 66.6 mmol) was added and the resulting mixture was stirred at room temperature for 30 minutes. Next, 2-(2-bromoethyl)-[1,3]dioxane (9.9 mL, 1.1 eq) was added ant the resulting mixture was heated at reflux for 40 hours. The reaction mixture was cooled to room temperature and then added ethyl acetate (150 mL) and with stirring acetic acid was added to pH=4, followed by dilution with water (100 mL) and ethyl acetate (150 mL). After partitioning, the layers were separated and then washed the organic layer with water (3×100 mL) and the ethyl acetate layers were dried over magnesium sulfate, filtered and concentrated to give the title compound as a colorless oil (16.91 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08318719B2
出典データセットuspto-grants-2012_11
ORD IDord-83be275999f24c53aa4056ecd01cbb9e
出典メモuspto-grants-2012_11