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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| 反応物 | 2,2-Dimethylbenzo[d][1,3]dioxole-5-carbaldehyde | HCID 596012 | — |
| 反応物 | Methyl2-(tert-butoxycarbonyl)-2-(dimethoxyphosphoryl)acetate | HCID 86599651 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 溶媒 | Ammonium Chloride | HCID 25517 | — |
| 生成物 | (Z)-methyl2-(tert-butoxycarbonyl)-3-(2,2-dimethylbenzo[d][1,3]dioxol-5-yl)acrylate | HCID 67163448 | 88.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08552181B2 |
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| 出典データセット | uspto-grants-2013_10 |
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| ORD ID | ord-49e0d37ba29c43e9b117bffc03743ae7 |
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| 出典メモ | uspto-grants-2013_10 |
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