Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 427555생성일: 2026년 10월 26일
Methyl 1-(pyridin-4-yl)piperidine-4-carboxylate → (1-(Pyridin-4-YL)piperidin-4-YL)methanol
https://huagongshe.com/reaction/427555
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methyl 1-(pyridin-4-yl)piperidine-4-carboxylate | HCID 12150696 | — |
| 반응물 | Aluminium lithium hydride | HCID 21226445 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (1-(Pyridin-4-YL)piperidin-4-YL)methanol | HCID 11310048 | 68.3% |
반응 단계
A solution of methyl N-(4-pyridyl)isonipecotate (600 mg, 2.72 mmol) in tetrahydrofuran was added to solution of lithium aluminum hydride (100 mg) in tetrahydrofuran (14 mL) cooled to 0° C. Upon consumption of the starting material (0.5-2 h), the mixture was treated with water (0.10 mL), 15% aqueous sodium hydroxide (0.10 mL), and water (0.30 mL). After 0.25 h, the mixture was sonicated for 0.25 h, then poured into a mixture of ethyl acetate, water, sodium tartrate, and potassium tartrate. The aqueous layer was extracted twice with ethyl acetate and the combined extracts were dried (magnesium sulfate), filtered, and concentrated in vacuo to yield 357 mg (68%) of the title compound, which was used without further purification.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06313122B1 |
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| 출처 데이터셋 | uspto-grants-2001_11 |
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| ORD ID | ord-b5e1b19ee4ef40d7b64c14433e8cf6d1 |
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| 출처 메모 | uspto-grants-2001_11 |
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