HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1466437Generated: October 31, 2026
Ethyl bromopyruvate → HCID 59251305, compound
https://huagongshe.com/reaction/1466437
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromopyruvate | HCID 66144 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 178438936 | HCID 178438936 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 59251305 | HCID 59251305 | 75.2% |
Reaction Steps
To a 250 mL round bottom flask attached with condenser was added N-(4-Bromo-phenyl)-2-isopropyl-benzamidine (1.94 g, 6.11 mmol), ethyl bromopyruvate (1.54 mL, 12.2 mmol), sodium bicarbonate (1.02 g, 12.2 mmol), and iso-propanol (45 mL). The reaction slurry was allowed to stir at 80° C. for approximately 2 hrs. The reaction solution was decanted into a clean round bottom flask and concentrated in vacuo. The resulting residue was dissolved in acetic acid (25 mL), and the solution was allowed to stir at reflux for approximately 2 hrs. The solution was concentrated in vacuo, and the product residue was taken into EtOAc (200 mL) and washed with aq NaCl (200 mL×2) and aq NaHCO3 (100 mL). The organic phase was partitioned, dried over Na2SO4, filtered, concentrated, and chromatographed through a 40 g SiO2 column using a mobile gradient of 100% Fix to 70% EtOAc to afford 1.90 g (75% yield) of title compound. MS (ES): 414.0 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09000022B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-81e00690868e403289a93aa97e75932e |
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| Source note | uspto-grants-2015_04 |
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