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HRID 13638作成日:2026年10月24日

Sodium Chloride → 2-(2'-Bromo-4-fluorophenoxy)tetrahydro-2H-pyran

https://huagongshe.com/ja/reaction/13638

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium ChlorideHCID 5234—
反応物3,4-dihydro-2H-pyranHCID 8080—
反応物Potassium CarbonateHCID 11430—
反応物Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
反応物2-Bromo-4-fluorophenolHCID 605472—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物2-(2'-Bromo-4-fluorophenoxy)tetrahydro-2H-pyranHCID 59340247—

反応手順

A mixture of 478.0 ml (5.24 mol) of 3,4-dihydropyran and 750 ml of dichloromethane was admixed with 65.4 g (260 mmol) of pyridinium p-toluenesulfonate. Subsequently, a solution of 500.0 g (2.62 mmol) of 2-bromo-4-fluorophenol in 500 ml of dichloromethane was added dropwise. After stirring for 24 h, the reaction mixture was admixed with a solution of 50 g of potassium carbonate in 500 ml of water, and then with 500 ml of saturated sodium chloride solution. The organic phase was removed, dried over potassium carbonate and, after freeing it of the solvent and potassium carbonate, fractionally distilled (approx. 1 mbar, top temperature from 79 to 82° C.) by means of a Vigreux column (40 cm). The product was obtained as a colorless, low-viscosity oil. The yield was 520.5 g (72.2%) at a purity of greater than 98.0% by 1H NMR.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728137B2
出典データセットuspto-grants-2010_06
ORD IDord-30441e9188ee410491001da6d20d30a7
出典メモuspto-grants-2010_06