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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1039664생성일: 2026년 10월 25일

1,8-Diazabicyclo(5.4.0)undec-7-ene → (Z)-methyl2-(tert-butoxycarbonyl)-3-(2,2-dimethylbenzo[d][1,3]dioxol-5-yl)acrylate

https://huagongshe.com/reaction/1039664

반응식

참여 물질

역할이름HCID투입량
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물2,2-Dimethylbenzo[d][1,3]dioxole-5-carbaldehydeHCID 596012—
반응물Methyl2-(tert-butoxycarbonyl)-2-(dimethoxyphosphoryl)acetateHCID 86599651—
용매DichloromethaneHCID 6344—
용매Ammonium ChlorideHCID 25517—
생성물(Z)-methyl2-(tert-butoxycarbonyl)-3-(2,2-dimethylbenzo[d][1,3]dioxol-5-yl)acrylateHCID 6716344888.9%

반응 단계

To a solution of methyl 2-(tert-butoxycarbonyl)-2-(dimethoxyphosphoryl)acetate (5255 mg, 17678 μmol) in 25 mL of DCM at 0° C. was added DBU (2665 μl, 17678 μmol) dropwise. To the mixture was then added a solution of 2,2-dimethylbenzo[d][1,3]dioxole-5-carbaldehyde (3000 mg, 16836 μmol) in 10 mL of DCM over 5 minutes so as to maintain internal temperature below 10° C. The reaction was warmed to rt and stiffed overnight before being diluted with DCM (25 mL) and poured in saturated ammonium chloride (100 mL). The aqueous layer was extracted with DCM (1×50 mL). The combined organic layers were washed with 10% aqueous sodium bicarbonate then water then brine and dried over Na2SO4. Concentration under reduced pressure and purification by silica gel provided (Z)-methyl 2-(tert-butoxycarbonyl)-3-(2,2-dimethylbenzo[d][1,3]dioxol-5-yl)acrylate (5005 mg, 85.1% yield) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08552181B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-49e0d37ba29c43e9b117bffc03743ae7
출처 메모uspto-grants-2013_10