HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 11571Generated: October 25, 2026
Acetamidomalonic acid diethyl ester → Diethyl 2-acetylamino-2-(2-methoxy-6-nitrobenzyl)malonate
https://huagongshe.com/reaction/11571
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetamidomalonic acid diethyl ester | HCID 14041 | — |
| Reactant | Benzene, 2-(bromomethyl)-1-methoxy-3-nitro- | HCID 186047 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Diethyl 2-acetylamino-2-(2-methoxy-6-nitrobenzyl)malonate | HCID 21974615 | 80.8% |
Reaction Steps
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).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07098235B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-f049805b02c647ba9683e13a05b400db |
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| Source note | uspto-grants-2006_08 |
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