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HRID 1044406作成日:2026年10月25日

Isobutylene oxide → 1-(4-Bromo-2-methoxyphenoxy)-2-methylpropan-2-ol

https://huagongshe.com/reaction/1044406

反応式

関与物質

役割名称HCID仕込み量
反応物Isobutylene oxideHCID 11208—
反応物Potassium CarbonateHCID 11430—
反応物Trisodium PhosphateHCID 24243—
反応物4-Bromo-2-methoxyphenolHCID 262234—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
溶媒AcetonitrileHCID 6342—
溶媒Ethyl AcetateHCID 8857—
生成物1-(4-Bromo-2-methoxyphenoxy)-2-methylpropan-2-olHCID 5959504992.1%

反応手順

A mixture of 4-bromo-2-methoxyphenol (8 g, 39.4 mmol), 2,2-dimethyloxirane (14 mL, 158 mmol), potassium carbonate (4.3 g, 35.5 mmol), and sodium phosphate, monobasic (4.25 g, 35.5 mmol) in acetonitrile and water (85:15, 100 mL) was stirred in a steel bomb at 150-165° C. for 8 h. The reaction was cooled to RT, diluted with ether and EtOAc (1:1), washed with 1N NaOH, dried (Na2SO4), and concentrated. The crude was passed through a pad of silica gel using EtOAc for elution to afford the desired product 1-(4-bromo-2-methoxyphenoxy)-2-methylpropan-2-ol 9A (10 g, 36.3 mmol, 92% yield) as a brown oil. 1H NMR (400 MHz, Chloroform-d) δ6.95-7.08 (2H, m), 6.77 (1H, d, J=8.28 Hz), 3.85 (3H, s), 3.79 (2H, s), 1.34 (6H, s).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08563583B2
出典データセットuspto-grants-2013_10
ORD IDord-9121703c7ed543eab7622c8c1dfd3050
出典メモuspto-grants-2013_10