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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1181033Generated: November 3, 2026

Ethylene carbonate → HCID 5018216, compound

https://huagongshe.com/reaction/1181033

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene carbonateHCID 7303—
Reactant3-Methyl-5-phenyl-1H-pyrazoleHCID 18774—
ReactantSodium hydrideHCID 24758—
SolventDimethylformamideHCID 6228—
ProductHCID 5018216HCID 501821659.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

Sodium hydride (2.5 g, 1.5 g NaH, 62 mmol, 1.1 equiv) was added over a period of 3 min to a solution of 5-methyl-3-phenyl-1H-pyrazole (9.00 g, 56.9 mmol, 1 equiv) in DMF (90 mL) cooled to 0° C. in an ice bath. After stirring 15 min, ethylene carbonate (7.6 mL, 10 g, 110 mmol, 2.0 equiv) was added. The bath was removed, and the reaction mixture was stirred for 15 h. The mixture was treated with 4 M aq K2CO3 (90 mL), heated at reflux for 5 h, and diluted with H2O (200 mL). After allowing the hot mixture to cool for 15 min, more H2O (100 mL) and then hexanes (100 mL) were added. The mixture was shaken vigorously and then allowed to separate. Crystals formed and stayed with the top organic layer. The aqueous layer was separated, and the crystals were collected by vacuum filtration and washed with hexanes (2×50 mL). The crystals were dissolved in Et2O/EtOAc (1:1; 200 mL), and the solution was dried (Na2SO4), filtered, and concentrated (75° C.) to give the title compound as an off-white crystalline solid (6.86 g, 59.6%). HRMS Calculated for C12H15N2O: m/z 203.1184. Found: 203.1168.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07282501B2
Source datasetuspto-grants-2007_10
ORD IDord-2b8e494616fb442fa4ea4ab00c47c6d0
Source noteuspto-grants-2007_10