HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bis-(1H-imidazol-2-YL)-methanone → ethyl (4R)-2-oxo-1,3-thiazolidine-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bis-(1H-imidazol-2-YL)-methanone | HCID 5250894 | — |
| Reactant | HCID 10964674 | HCID 10964674 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | ethyl (4R)-2-oxo-1,3-thiazolidine-4-carboxylate | HCID 477571 | 169.2% |
Reaction Steps
To a solution of 3-1 (8.5 g, 22.6 mmol) in 200 mL THF was added of carbonyl diimidazole (12.5 g) and the solution was stirred overnight at room temperature. The solution was concentrated in vacuo, 200 mL of 5% Na2CO3 was added and the solution stirred for one hour whereupon 6M HCl was added until the pH of the solution remained at 2. The solution was extracted with EtOAc, the organic phases were then combined, dried over MgSO4, filtered and concentrated in vacuo. The compound was purified by flash chromatography using 40% EtOAc/hexanes to yield 6.7 g of 3-2 as a colorless oil. 1H NMR (400 MHz, acetone-d6): δ 7.5 (br s, 1H), 4.5 (dd, 1H), 4.2 (q, 2H), 3.8 (dd, 1H), 3.6 (dd, 1H), 1.2 (t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07109223B2 |
| Source dataset | uspto-grants-2006_09 |
| ORD ID | ord-8db284ef410640a9afa0edb4ec88ab74 |
| Source note | uspto-grants-2006_09 |