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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 412052생성일: 2026년 10월 23일

Water → 4-Phenyl-1-(3'-sulfopropyl)-1,2,3,6 tetrahydropyridine

https://huagongshe.com/ko/reaction/412052

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물4-PhenylpyridineHCID 13651—
반응물Propane sultoneHCID 14264—
반응물Sodium borohydrideHCID 4311764—
용매AcetoneHCID 180—
용매MethanolHCID 887—
생성물4-Phenyl-1-(3'-sulfopropyl)-1,2,3,6 tetrahydropyridineHCID 981790693%

반응 단계

To a solution of 4-phenylpyridine (15.5 g, 0.1 mol) in acetone (100 mL) was added 1,3-propane sultone (12.2 g, 0.1 mol) at room temperature. The mixture was then heated at reflux temperature overnight. The resultant suspension was cooled to room temperature. The solid was collected by filtration and washed with acetone. To a solution of the solid (31 g) in methanol (500 mL) was added sodium borohydride (10 g, 260 mmol) portionwise, and the mixture was stirred at room temperature for 2 h. Distilled water (50 mL) was added to destroy the excess of sodium borohydride. The mixture was diluted with methanol (200 ml), and neutralized with Amberlite IR-120 ion-exchange resin (H+ form, 300 g). A white precipitate was formed. The precipitate and the resin were removed by filtration and treated with distilled water (400 mL) at ˜100 ° C. The mixture was filtered and the residual resin was washed with hot distilled water (2×200 mL). The filtrates and washings were combined and concentrated to dryness. The residue was co-evaporated with methanol (3×200 mL), and then recrystallized from ethanol-water {8:2 (v/v)} to afford 4-phenyl-1-(3′-sulfopropyl)-1,2,3,6-tetrahydropyridine as white crystals (26 g, 93%). The 1H and 13C NMR spectra were in agreement with the structure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06562836B1
출처 데이터셋uspto-grants-2003_05
ORD IDord-172ea02c9ec545a6b257880452a2c0f0
출처 메모uspto-grants-2003_05