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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1836457생성일: 2026년 10월 26일

Acetic Acid → (2,2-Dimethyl-5-oxo-[1,3]dioxolan-4-ylidene)-acetic acid

https://huagongshe.com/reaction/1836457

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Tetrabutylammonium FluorideHCID 2724141—
반응물(Z)-2,2-dimethyl-5-(tert-butyldimethylsilyloxycarbonylmethylene)-1,3-dioxolan-4-oneHCID 60104830—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물(2,2-Dimethyl-5-oxo-[1,3]dioxolan-4-ylidene)-acetic acidHCID 6886064262%

반응 단계

The crude (Z)-2,2-dimethyl-5-(tert-butyldimethylsilyloxycarbonylmethylene)-1,3-dioxolan-4-one (72.4 mmol) in tetrahydrofuran (50 ml) was treated at 22° C. with acetic acid (13 ml, 0.227 mmol) followed by 73 ml (73.0 mmol) of a 1M solution of tetrabutylammonium fluoride in tetrahydrofuran. After 1 h at 22° C., the reaction mixture was diluted with ethyl acetate (500 ml), washed with water, brine and dried (anhydrous magnesium sulfate). Evaporation of the solvent under reduced pressure and trituration of the residual solid with toluene (50 ml) gave 7.70 g (62% yield for 3 steps) of the title Z-isomer as a white crystalline solid. Concentration of the mother liquors yielded another 0.2 g of a 75:25 mixture of Z and E isomers. Z-Isomer; 1H NMR (400 MHz, CDCl3) δ: 1.78 (s, 3), 5.89 (s, 1). E-Isomer: 1H NMR (400 MHz, CDCl3) δ: 1.80 (s, 3), 6.03 (s, 1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06777440B2
출처 데이터셋uspto-grants-2004_08
ORD IDord-4a02acb295164b139664d66e794b12be
출처 메모uspto-grants-2004_08