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HRID 584718作成日:2026年10月26日

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

https://huagongshe.com/reaction/584718

反応式

関与物質

役割名称HCID仕込み量
反応物4-Methylbenzyl chlorideHCID 7722—
反応物Potassium CarbonateHCID 11430—
反応物Piperidin-4-olHCID 79341—
溶媒tert-ButanolHCID 6386—
生成物1-(4-Methylbenzyl)piperidin-4-olHCID 79148252%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06927225B2
出典データセットuspto-grants-2005_08
ORD IDord-be1a1e9e8c574f94b5d0b79430183cfa
出典メモuspto-grants-2005_08