참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetamidomalonic acid diethyl ester | HCID 14041 | — |
| 반응물 | Benzene, 2-(bromomethyl)-1-methoxy-3-nitro- | HCID 186047 | — |
| 반응물 | Sodium | HCID 5360545 | — |
| 용매 | Ethanol | HCID 702 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | Diethyl 2-acetylamino-2-(2-methoxy-6-nitrobenzyl)malonate | HCID 21974615 | 80.8% |
반응 단계
Sodium metal (1.15 g) was dissolved in absolute ethanol (500 mL), and to the resulting solution was added diethyl 2-acetylaminomalonate (9.1 g). After 15 min at room temperature, a solution of 2-methoxy-6-nitrobenzyl bromide (J. Med. Chem. 1977, 20, 190–196) (8.6 g) in tetrahydrofuran (25 mL) was added over 2 min. After 16 h stirring at room temperature the mixture was evaporated. The residue was dissolved in a mixture of ethyl acetate and water. The ethyl acetate layer was separated and washed sequentially with water and brine before drying over anhydrous sodium sulfate. Evaporation was followed by silica gel chromatography eluting initially with dichloromethane, followed by ethyl acetate, to obtain diethyl 2-acetylamino-2-(2-methoxy-6-nitrobenzyl)malonate (10.8 g).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07098235B2 |
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| 출처 데이터셋 | uspto-grants-2006_08 |
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| ORD ID | ord-f049805b02c647ba9683e13a05b400db |
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| 출처 메모 | uspto-grants-2006_08 |
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