돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 46541생성일: 2026년 10월 24일

Tert-butyl acetoacetate → Methyl 4-tert-butoxycarbonyl-3-dimethoxymethyl-5-oxohexanoate

https://huagongshe.com/ko/reaction/46541

반응식

참여 물질

역할이름HCID투입량
반응물Tert-butyl acetoacetateHCID 15538—
반응물Potassium FluorideHCID 522689—
반응물methyl (2Z)-4,4-dimethoxy-2-butenoateHCID 12283105—
용매tert-ButanolHCID 6386—
생성물Methyl 4-tert-butoxycarbonyl-3-dimethoxymethyl-5-oxohexanoateHCID 20396638—

반응 조건

온도100 °C

반응 단계

Into a 500-ml reactor are placed 40 g of potassium fluoride, 40 ml of dry tert-butanol, 123 g of methyl cis-4,4-dimethoxy-2-butenate and 36 g of tert-butyl acetoacetate. The mixture is heated at 100° C. with stirring on an oil bath for two days. On completion of the reaction, the tert-butanol is distilled off from the mixture. The residue is dissolved in ethyl acetate, and the solution washed with an aqueous solution of common salt and then dried. The solvent is removed from the product. The resulting residue is purified by a silica gel column and distilled at reduced pressure, giving methyl 4-tert-butoxycarbonyl-3-dimethoxymethyl-5-oxohexanoate (compound (5), R1 =t-Bu, R2 =R3 =CH3) in a yield of 95.4%, b.p. 72°-76° C./0.014 mm Hg.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04173707
출처 데이터셋uspto-grants-1979_11
ORD IDord-6ea2e3098a98444b92423b26c3fe1be2
출처 메모uspto-grants-1979_11