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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 869785생성일: 2026년 10월 26일

Triethylamine → (E)-tert-butyl 4-(4-methoxy-4-oxobut-2-enoyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/869785

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Oxalyl chlorideHCID 65578—
반응물tert-Butyl piperazine-1-carboxylateHCID 143452—
반응물(E)-4-methoxy-4-oxobut-2-enoateHCID 21721168—
촉매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물(E)-tert-butyl 4-(4-methoxy-4-oxobut-2-enoyl)piperazine-1-carboxylateHCID 6731231721%

반응 단계

Mono methyl fumarate (650 mg, 5.0 mmol) was taken up in 10 mL of CH2Cl2 and oxalyl chloride (420 μL, 5.0 mmol) was added. After a few drops of DMF was added, the reaction mixture was stirred at room temperature until all gas evolution had ceased (1 h). This freshly prepared solution of acid chloride was then added dropwise at 0° C. to a solution containing Boc-piperazine (930 mg) and triethylamine (1.0 mL, 7.5 mmol) in 20 mL of CH2Cl2. The resulting reaction mixture was stirred at room temperature for 1 h and washed with brine. The organic layer was dried (Na2SO4) and concentrated under reduced pressure. Purification by chromatography (CH2Cl2) afforded 310 mg of (E)-tert-butyl 4-(4-methoxy-4-oxobut-2-enoyl)piperazine-1-carboxylate (21% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08969354B2
출처 데이터셋uspto-grants-2015_03
ORD IDord-600d3d67568f492d99d760ca17391ec9
출처 메모uspto-grants-2015_03