HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 539012Generated: October 30, 2026
Triethylamine → (S)-3-(2,4-dimethoxybenzyl)-5-isopropylimidazolidine-2,4-dione
https://huagongshe.com/reaction/539012
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (S)-methyl 2-(3-(2,4-dimethoxybenzyl)ureido)-3-methylbutanoate | HCID 2012917 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (S)-3-(2,4-dimethoxybenzyl)-5-isopropylimidazolidine-2,4-dione | HCID 67033852 | 71% |
Reaction Steps
A solution of (S)-methyl 2-(3-(2,4-dimethoxybenzyl)ureido)-3-methylbutanoate (1.00 g, 3.10 mmol) in MeOH (7.5 mL) and NEt3 (0.430 mL, 3.10 mmol) in a sealed vessel was placed in preheated sand bath (at 100° C.) and heated for 18 hours. The cooled reaction mixture was concentrated and the residue was taken up in ether, washed with water, dried over sodium sulfate and filtered. Purification of the crude material by column chromatography, eluting with 1-3% MeOH/dichloromethane, afforded (S)-3-(2,4-dimethoxybenzyl)-5-isopropylimidazolidine-2,4-dione as an ivory colored solid (0.640 g, 71%). LCMS (APCI+) m/z 293 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08865726B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-550b81a359bd43658762b9d7412ba734 |
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| Source note | uspto-grants-2014_10 |
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