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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2190080Generated: November 1, 2026

Acetonitrile → 4-chloro-5-ethyl-6,7-dihydro-5H-cyclopenta[d]pyrimidine

https://huagongshe.com/reaction/2190080

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantHCID 178435582HCID 178435582—
Product4-chloro-5-ethyl-6,7-dihydro-5H-cyclopenta[d]pyrimidineHCID 8665181126.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

Phosphorous oxychloride (1.92 mL, 20.6 mmol) was added to a solution of 5-ethyl-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-ol (1.13 g, 6.88 mmol) in acetonitrile (40 mL, 766 mmol) and heated to 80° C. The reaction was stirred at 80° C. for 15 hours. LCMS confirmed consumption of the starting material peak and conversion to a new product peak. The reaction was cooled to room temperature and concentrated under vacuum. The residue was partitioned between DCM and saturated aqueous NaHCO3. The organic layer was dried over anhydrous Na2SO4. The crude solution was concentrated under vacuum to an oil. The crude was purified by silica gel chromatography (gradient: 10-50% EtOAc/Hexanes). Purification provided 4-chloro-5-ethyl-6,7-dihydro-5H-cyclopenta[d]pyrimidine (334 mg, 1.83 mmol, 26.6% yield) as an oil. MS (APCI+) [M+H]: 183.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324221B2
Source datasetuspto-grants-2012_12
ORD IDord-ec586296420e4aafa0be988dc33a670e
Source noteuspto-grants-2012_12