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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2383794Generated: October 26, 2026

Ethyl Acetate → 1-Benzothiazol-6-yl-imidazolidin-2-one

https://huagongshe.com/reaction/2383794

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
Reactant1-Benzothiazol-6-yl-3-(2-chloro-ethyl)-ureaHCID 68783928—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product1-Benzothiazol-6-yl-imidazolidin-2-oneHCID 6667855499.1%

Reaction Steps

1-Benzothiazol-6-yl-3-(2-chloro-ethyl)-urea (I-84a: 2.7 g, 10.58 mmol) in dry DMF (80 mL) was added dropwise to a stirred mixture of sodium hydride (0.76 g, 31.74 mmol) in THF (100 mL) over a period of 20 minutes at 0° C. under nitrogen atmosphere. The reaction mixture was stirred at room temperature for 2 hours. The reaction was monitored by TLC (100% ethyl acetate). The reaction mixture was quenched with MeOH (6 mL), concentrated under reduced pressure, followed by the addition of ice. The precipitate was collected and dried under reduced pressure to afford 2.3 g (85.18% yield) of 1-benzothiazol-6-yl-imidazolidin-2-one as the required product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263635B2
Source datasetuspto-grants-2012_09
ORD IDord-bbf10c375dae4ef29ad8ad5afde83a47
Source noteuspto-grants-2012_09