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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 277157생성일: 2026년 10월 24일

4-Methylbenzyl chloride → 1-(4-Methylbenzyl)piperidin-4-ol

https://huagongshe.com/ko/reaction/277157

반응식

참여 물질

역할이름HCID투입량
반응물4-Methylbenzyl chlorideHCID 7722—
반응물Potassium CarbonateHCID 11430—
반응물Piperidin-4-olHCID 79341—
용매tert-ButanolHCID 6386—
생성물1-(4-Methylbenzyl)piperidin-4-olHCID 79148251.6%

반응 단계

Synthesis of this compound was accomplished according to Scheme 33. To 5.05 g (50 mmol) of 4-hydroxypiperidine and 7.08 g (50 mmol) of p-methylbenzyl chloride in 25 mL of tert-butanol was added excess solid potassium carbonate, and the mixture was heated on a steam bath for 3 h. The mixture was cooled to room temperature and partitioned between ether and water. The organic phase was extracted with cold dilute HCl, and the acidic aqueous phase was extracted with ether twice. The aqueous phase was made basic with ice and 50% aqueous NaOH and extracted with ether. The ether phase was washed with dilute aqueous sodium bicarbonate solution, brine, dried, and evaporated under vacuum to give 5.3 g (52) of 1-(4-methylbenzyl)-4-hydroxypiperidine (123) as an oil. GC/MS showed 100% purity with a molecular ion of 205.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06355660B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-40bf85493a0040dfb069d802b5653eb2
출처 메모uspto-grants-2002_03