HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1249682Generated: October 31, 2026
Ethyl bromoacetate → 5-Octyl-5-(ethoxycarbonylmethyl)barbituric acid
https://huagongshe.com/reaction/1249682
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Octyl barbituric acid | HCID 260794 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-Octyl-5-(ethoxycarbonylmethyl)barbituric acid | HCID 9862142 | — |
Reaction Steps
4.05 g of 5-octylbarbituric acid (preparation 7) are dissolved in 25 ml of dimethylformamide, 1.16 g of sodium carbonate are added. Ethyl bromoacetate (2.25 ml) is added dropwise to the reaction mixture in 5 minutes, then the mixture is kept at room temperature under stirring for about 3 hours. The reaction mixture is then partitioned between 400 ml of water, 17 ml of 1 N hydrochloric acid and 150 ml of ethyl acetate. The organic phase is separated and washed with 150 ml of water and 100 ml of brine, then it is dried over sodium sulfate. The aqueous phases are extracted with 100 ml of ethyl acetate and the organic extracts are pooled, dried over sodium sulfate and evaporated to dryness, to give 6.5 g an oily residue. This residue is purified by silica gel chromatography (eluant methylene chloride/ethyl acetate 9 1) to give 3.87 g of the product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06335332B1 |
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| Source dataset | uspto-grants-2002_01 |
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| ORD ID | ord-3c3411771cd94c18a68188968c511f97 |
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| Source note | uspto-grants-2002_01 |
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