Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2200257Generated: November 1, 2026

m-Chloroperbenzoic acid → 4-chloro-6,7-dihydro-5H-cyclopenta[d]pyrimidine 1-oxide

https://huagongshe.com/reaction/2200257

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant4-chloro-5H,6H,7H-cyclopenta[d]pyrimidineHCID 13312449—
SolventChloroformHCID 6212—
Product4-chloro-6,7-dihydro-5H-cyclopenta[d]pyrimidine 1-oxideHCID 1423109147%

Reaction Steps

To a solution of 4-chloro-6,7-dihydro-5H-cyclopenta[d]pyrimidine (5.69 g, 36.8 mmol) in chloroform (200 mL) was added MCPBA (19 g, 84.8 mmol) in chloroform (50 mL) dropwise. The mixture was stirred at room temperature for 16 hour. After cooling with ice-water, the mixture was quenched with Na2S2O3 (27.5 g) in water (110 mL) dropwise and followed by Na2CO3 (14 g) in water (52 mL) dropwise. The organic phase was separated and the aqueous phase was extracted with chloroform (3×200 mL). The organic phase was dried and concentrated at low temperature (<25° C.). The residue was subject to chromatography on silica gel, eluting by ethyl acetate to afford 4-chloro-6,7-dihydro-5H-cyclopenta[d]pyrimidine 1-oxide (2.93 g, 47%). MS (APCI+) [M+H] +171.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359340B2
Source datasetuspto-grants-2016_06
ORD IDord-0a89fcc56d174e40865d58113640be8f
Source noteuspto-grants-2016_06