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HRID 46305作成日:2026年10月25日

Sulfuric Acid → 2-Iodo-4-(trifluoromethyl)phenol

https://huagongshe.com/reaction/46305

反応式

関与物質

役割名称HCID仕込み量
反応物Sulfuric AcidHCID 1118—
反応物4-(Trifluoromethyl)phenolHCID 67874—
反応物N-IodosuccinimideHCID 120273—
触媒N-IodosuccinimideHCID 120273—
溶媒Acetic AcidHCID 176—
生成物2-Iodo-4-(trifluoromethyl)phenolHCID 11572816242.7%

反応条件

温度0 °C

反応手順

N-iodosuccinimide (69.5 g, 0.309 moles) was suspended in acetic acid (257 mL) and cooled to 0° C. 4-Trifluoromethylphenol (50.0 g, 0.310 moles) was added followed by sulphuric acid (5.44 mL) dropwise over 5 minutes. The orange-brown suspension was stirred whist warming slowly to room temperature over 18 hours. A further portion of N-iodosuccinimide (2.5 g, 0.011 moles) was added and the mixture was stirred at room temperature for 24 hours. The reaction was quenched by adding water (150 mL) and extracted with dichloromethane (2×100 mL). The combined organics were washed with a saturated aqueous solution of sodium metabisulphite (2×50 mL) and then with saturated aqueous sodium chloride solution (50 mL). The organics were dried over anhydrous magnesium sulphate, filtered and the solvents removed in vacuo to give the crude title product as a light yellow oil. This batch was combined with the products from two further identical reactions and purified by distillation in vacuo. The product was collected boiling at approximately 45° C. at 2 mBar to give the title compound as a pink-orange semi-solid (216 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08541588B2
出典データセットuspto-grants-2013_09
ORD IDord-4e13e72a21344c4f9c57a1d93514f927
出典メモuspto-grants-2013_09