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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2215081Generated: November 1, 2026

Bis-(1H-imidazol-2-YL)-methanone → ethyl (4R)-2-oxo-1,3-thiazolidine-4-carboxylate

https://huagongshe.com/reaction/2215081

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBis-(1H-imidazol-2-YL)-methanoneHCID 5250894—
ReactantHCID 10964674HCID 10964674—
SolventTetrahydrofuranHCID 8028—
Productethyl (4R)-2-oxo-1,3-thiazolidine-4-carboxylateHCID 477571169.2%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07109223B2
Source datasetuspto-grants-2006_09
ORD IDord-8db284ef410640a9afa0edb4ec88ab74
Source noteuspto-grants-2006_09