Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1789797생성일: 2026년 10월 27일
Potassium Hydroxide → 2-(2-Tert-butoxycarbonylamino-pyridin4-ylmethyl)-malonic acid monoethyl ester
https://huagongshe.com/reaction/1789797
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Potassium Hydroxide | HCID 14797 | — |
| 반응물 | 2-(2-Tert-butoxycarbonylamino-pyridin4-ylmethyl)-malonic acid diethyl ester | HCID 54557970 | — |
| 용매 | Ethanol | HCID 702 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 2-(2-Tert-butoxycarbonylamino-pyridin4-ylmethyl)-malonic acid monoethyl ester | HCID 54548642 | 81.3% |
반응 단계
A solution of KOH (0.19 g, 3.43 mmol) in ethanol (5 mL) was added to a solution of 2-(2-tert-butoxycarbonylamino-pyridin4-ylmethyl)-malonic acid diethyl ester (1.20 g, 3.27 mmol) in ethanol (5 mL) and methylene chloride (5 mL) at 0° C. The mixture was stirred for 18 h at room temperature. The mixture was concentrated under reduced pressure and water was added to the residue. The aqueous layer was washed with diethyl ether, acidified to pH 4 by 1M HCl, and extracted with methylene chloride. The organic layer was washed with water, brine and dried. After filtration and evaporation in vacuo, the crude product was purified by flash chromatography (CH3OH/CH2Cl2, 1:20) to yield 2-(2-tert-butoxycarbonylamino-pyridin4-ylmethyl)-malonic acid monoethyl ester (0.90 g, 81%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07071175B1 |
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| 출처 데이터셋 | uspto-grants-2006_07 |
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| ORD ID | ord-d245cc3b73f8448fb111e6ba4a53d5dd |
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| 출처 메모 | uspto-grants-2006_07 |
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