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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 538726Generated: October 29, 2026

Ethyl Acetate → HCID 57841185, compound

https://huagongshe.com/reaction/538726

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
ReactantIodocyclopentaneHCID 73784—
ReactantHCID 178450770HCID 178450770—
SolventDimethylformamideHCID 6228—
ProductHCID 57841185HCID 5784118570.4%

Reaction Steps

To tert-Butyl 3-(4-phenoxyphenyl)-1H-pyrazole-4-carboxylate (15.6 mg, 0.46 mmol) in N,N-dimethylformamide (2 mL) was added sodium hydride, 60% in mineral oil (20.8 μg, 0.52 mmol). After the gas evolution ceased (about 5 minutes), cyclopentyl iodide (59 μL, 0.51 mmol) was added dropwise and the mixture was stirred for 16 hours at room temperature. EtOAc was added and the crude mixture was washed with a saturated aqueous solution of NaHCO3. The aqueous phase was further extracted with EtOAc (3 times). The combined organic extracts were washed with water and brine. The organics were dried (MgSO4), filtered and concentrated in vacuo. The residue was purified by silica gel chromatography (eluting with petroleum ether/DCM) to afford the title compound as a white solid (0.131 g, 69% yield). MS (ES+) m/e=405. 1H NMR (CDCl3) δH 1.51 (9H, s), 1.70-1.80 (2H, m), 1.85-2.00 (2H, m), 2.02-2.13 (2H, m), 2.18-2.30 (2H, m), 4.71 (1H, quint.), 7.06 (4H, d), 7.12 (1H, t), 7.35 (2H, t), 7.76 (2H, d), 7.95 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865751B2
Source datasetuspto-grants-2014_10
ORD IDord-b805f6b5c3404c3fa911ffe4a1db4b60
Source noteuspto-grants-2014_10