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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 744706생성일: 2026년 10월 24일

Cyclopropanecarboxaldehyde → trans-N-methyl-N-methoxy-3-cyclopropylpropenamide

https://huagongshe.com/ko/reaction/744706

반응식

참여 물질

역할이름HCID투입량
반응물CyclopropanecarboxaldehydeHCID 123114—
반응물Diethyl (N-methoxy-N-methylcarbamoylmethyl)phosphonateHCID 2773719—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물trans-N-methyl-N-methoxy-3-cyclopropylpropenamideHCID 1103005394%

반응 조건

온도-78 °C

반응 단계

To a solution of N-methoxy-N-methyl diethylphosphonoacetamide (34.56 g, 144.5 mmol) in THF (200 mls) at -78° C., was added n-butyllithium (57.8 mls of a 2.5M solution in hexanes, 144.5 mmol) dropwise. Upon completion of addition, the mixture was stirred for 30 mins at -78° C. A solution of cyclopropanecarboxaldehyde (6.75 g, 96.3 mmol) in THF (50 mls) was then added dropwise. Upon completion of addition, the cooling bath was withdrawn and the reaction allowed to warm to r.t. It was then diluted with aqueous sat'd NH4Cl (200 mls) and the THF was stripped off in vacuo. The aqueous residue was extracted with ethylacetate (3×200 mls). The organics were combined, dried with MgSO4 and concentrated. The resulting residue was chromatographed (silica gel, ether:hexanes, 3:2) to afford 14.09 g (94%) of trans-N-methyl-N-methoxy-3-cyclopropylpropenamide as a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05559144
출처 데이터셋uspto-grants-1996_09
ORD IDord-e7c14a57a20044edab54869ee8b15d7d
출처 메모uspto-grants-1996_09