HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 893093Generated: October 26, 2026
2,3-Dibromopropene → Diethyl (2-Bromoallyl)acetamidomalonate
https://huagongshe.com/reaction/893093
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,3-Dibromopropene | HCID 10552 | — |
| Reactant | Acetamidomalonic acid diethyl ester | HCID 14041 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Diethyl (2-Bromoallyl)acetamidomalonate | HCID 53941200 | 89.5% |
Reaction Steps
To a stirred mixture of diethyl acetaminomalonate (217 g, 1.0 mol) and 2,3-dibromopropene (240 g, 1.2 mol) in dry tetrahydrofuran (2.50 L), under nitrogen, was added sodium hydride (26.4 g, 1.1 mol) in several portions. The reaction mixture was stirred at room temperature for 30 min, then heated to reflux. After heating for 18 h, the resultant slurry was cooled to room temperature and suction filtered through a short pad of silica gel. The solid rescue as washed with tetrahydrofuran (2×50 mL), and the filtrates were combined and concentrated. The residue was dissolved in ethyl acetate (2.0 L), washed with water and brine, and then was dried over MgSO4. Filtration and concentration gave a yellow oil which solidified upon drying. The resultant solid was recrystallized from a mixture of hot ethyl acetate/hexane to give 301 g (89%) of the desired product: m.p. 85-87° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05122514 |
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| Source dataset | uspto-grants-1992_06 |
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| ORD ID | ord-4d9ed753a79f4570b6ed291d4cf151da |
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| Source note | uspto-grants-1992_06 |
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