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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 13638생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Sodium ChlorideHCID 5234—
반응물3,4-dihydro-2H-pyranHCID 8080—
반응물Potassium CarbonateHCID 11430—
반응물Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
반응물2-Bromo-4-fluorophenolHCID 605472—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물2-(2'-Bromo-4-fluorophenoxy)tetrahydro-2H-pyranHCID 59340247—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728137B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-30441e9188ee410491001da6d20d30a7
출처 메모uspto-grants-2010_06