HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1980293Generated: October 26, 2026
tert-Butanol → 1-benzyl 5-tert-butyl (5S)-2-oxoimidazolidine-1,5-dicarboxylate
https://huagongshe.com/reaction/1980293
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | (S)-(-)-2-Oxo-1,5-imidazolidinedicarboxylic acid 1-benzyl ester | HCID 688196 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 1-benzyl 5-tert-butyl (5S)-2-oxoimidazolidine-1,5-dicarboxylate | HCID 11067160 | 89% |
Reaction Steps
5.1 g of (4S)-3-benzyloxycarbonyl-2-oxo-imidazolidine-4-carboxylic acid (Liebich's Annalen der Chemie 529 (1937), page 1) are dissolved in 20 ml of pyridine, and 50 ml of tert.-butanol are added thereto. The solution is cooled to a temperature below -5° C., and 3.5 g of phosphorous oxychloride are added dropwise thereto. The mixture is stirred at the same temperature for about 30 minutes and then at room temperature for 3 hours. The reaction mixture is poured into 200 ml of ice-water, and extracted with ethyl acetate. The extract is washed with 1% hydrochloric acid, an aqueous sodium bicarbonate solution and water, successively. Then, the extract is dried and evaporated to remove solvent. The residue obtained is crystallized with a mixture of ether and n-hexane. 5.5 g of tert.-butyl (4S)-3-benzyloxycarbonyl-2-oxo-imidazolidine-4-carboxylate are obtained as colorless crystals. Yield: 89.0%
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04508727 |
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| Source dataset | uspto-grants-1985_04 |
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| ORD ID | ord-7ab2beeafb4b4018b5a1036bb6132983 |
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| Source note | uspto-grants-1985_04 |
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