HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1033108Generated: October 26, 2026
Ethyl 2-(butylamino)acetate → 1-Butylimidazolidine-2,4-dione
https://huagongshe.com/reaction/1033108
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 2-(butylamino)acetate | HCID 10607047 | — |
| Reactant | Potassium cyanate | HCID 11378442 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 1-Butylimidazolidine-2,4-dione | HCID 118506 | 68% |
Reaction Steps
A quantity of 24.4 g (0.30 mole) of potassium cyanate is added portionwise, at room temperature, to a stirred solution of 31.80 g (0.20 mole) of ethyl N-butylglycinate in 220 mL (0.22 mole) of 1N hydrochloric acid. The solution is warmed to ca. 90° C. (at ca. 50° C. an oil separates). After 10 minutes at 90° C., concentrated hydrochloric acid (250 mL) is cautiously added over 2 minutes and the resulting solution is heated at 90°-100° C. for 1/2 hour. The solution is concentrated at reduced pressure to dryness. The last amounts of water are chased by addition and removal of 3×100 mL of absolute ethanol. The residue is extracted with 400 mL 50% ethanolmethylene chloride. The inorganics are filtered and the filtrate is concentrated to dryness. Trituration of the residue with 100 mL of water and filtration gives pure 1-butylhydantoin in 68% yield; mp 90°-92° C.; MS (EI) 156.1 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05308853 |
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| Source dataset | uspto-grants-1994_05 |
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| ORD ID | ord-f849cd47db634bf3aa1376ec38221271 |
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| Source note | uspto-grants-1994_05 |
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