돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 727125생성일: 2026년 10월 26일

Sodium hydride → 2-(3-Cyano-3-(3,4-dichlorophenyl)propyl)oxytetrahydropyran

https://huagongshe.com/reaction/727125

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물Ammonium ChlorideHCID 25517—
반응물(3,4-Dichlorophenyl)acetonitrileHCID 76690—
반응물2-(2-Bromoethoxy)tetrahydro-2H-pyranHCID 86621—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물2-(3-Cyano-3-(3,4-dichlorophenyl)propyl)oxytetrahydropyranHCID 1567080758.2%

반응 단계

20 g of a 55-60% dispersion of sodium hydride in oil are suspended in 200 ml of dry tetrahydrofuran. A solution of 85 g of 3,4-dichlorophenylacetonitrile in 500 ml of tetrahydrofuran is added dropwise at 20° C. over 30 minutes and the reaction mixture is then stirred at room temperature for 2 hours. A solution of 98 g of 2-bromoethoxytetrahydropyran in 100 ml of tetrahydrofuran is added to the resulting mixture cooled to -20° C., the mixture is allowed to warm up to room temperature and, after 2 hours, a solution of 50 g of ammonium chloride in 3 liters of water is added. Extraction is carried out with 1.5 liters of ethyl ether and the extract is washed with a saturated solution of sodium chloride, decanted, dried over MgSO4 and concentrated under vacuum. The residue is chromatographed on silica gel using dichloromethane as the eluent. The pure product fractions are concentrated under vacuum to give 83.6 g of an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05712288
출처 데이터셋uspto-grants-1998_01
ORD IDord-0b43a25277334b74b65fb8334e53155b
출처 메모uspto-grants-1998_01