참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | 4-Phenylpyridine | HCID 13651 | — |
| 반응물 | Propane sultone | HCID 14264 | — |
| 반응물 | Sodium borohydride | HCID 4311764 | — |
| 용매 | Acetone | HCID 180 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | 4-Phenyl-1-(3'-sulfopropyl)-1,2,3,6 tetrahydropyridine | HCID 9817906 | 93% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06562836B1 |
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| 출처 데이터셋 | uspto-grants-2003_05 |
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| ORD ID | ord-172ea02c9ec545a6b257880452a2c0f0 |
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| 출처 메모 | uspto-grants-2003_05 |
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