Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 54182생성일: 2026년 10월 24일
Diethyl 2-(ethoxymethylidene)-3-oxobutanedioate → Triethyl 1,6-dihydro-6-oxo-2,3,5-pyridinetricarboxylate
https://huagongshe.com/ko/reaction/54182
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diethyl 2-(ethoxymethylidene)-3-oxobutanedioate | HCID 40590 | — |
| 반응물 | Sodium Acetate | HCID 517045 | — |
| 반응물 | Ethylmalonamate | HCID 21894451 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | Triethyl 1,6-dihydro-6-oxo-2,3,5-pyridinetricarboxylate | HCID 19958207 | 80.3% |
반응 단계
A solution of ethylmalonamate (23.6 g, 0.18 mol) in absolute ethanol (300 mL) is added to a stirred solution of diethyl ethoxymethyleneoxalacetate (44.0 g, 0.18 mol) in ethanol (200 mL) at 0° C., followed by the addition, of solid sodium acetate (14.72 g, 0.18 mol). After stirring for ten minutes at 0° C., the mixture is heated to reflux and stirred for 13.5 hours. After cooling, the ethanol is removed under vacuum, and the residue diluted with water and acidified to pH 2 with concentrated hydrochloric acid. The aqueous solution is extracted with methylene chloride (2×200 mL) and the organic layer washed with 300 mL saturated sodium chloride, then dried over anhydrous magnesium sulfate and concentrated in vacuum to give 45.0 g of the title product as an orange oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05622913 |
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| 출처 데이터셋 | uspto-grants-1997_04 |
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| ORD ID | ord-e115c8113c62468c9cc104c1ac9af4d3 |
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| 출처 메모 | uspto-grants-1997_04 |
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