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HRID 1039664作成日:2026年10月26日

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

反応式

関与物質

役割名称HCID仕込み量
反応物1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
反応物2,2-Dimethylbenzo[d][1,3]dioxole-5-carbaldehydeHCID 596012—
反応物Methyl2-(tert-butoxycarbonyl)-2-(dimethoxyphosphoryl)acetateHCID 86599651—
溶媒DichloromethaneHCID 6344—
溶媒Ammonium ChlorideHCID 25517—
生成物(Z)-methyl2-(tert-butoxycarbonyl)-3-(2,2-dimethylbenzo[d][1,3]dioxol-5-yl)acrylateHCID 6716344888.9%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08552181B2
出典データセットuspto-grants-2013_10
ORD IDord-49e0d37ba29c43e9b117bffc03743ae7
出典メモuspto-grants-2013_10