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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 408530Generated: October 29, 2026

Hydrogen Peroxide → HCID 11524855, compound

https://huagongshe.com/reaction/408530

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantWaterHCID 962—
ReactantDiethyl EtherHCID 3283—
ReactantHCID 11582446HCID 11582446—
SolventAcetic AcidHCID 176—
ProductHCID 11524855HCID 1152485536.6%

Reaction Conditions

Temperature85 °C

Reaction Steps

1-(4-Methoxy-phenyl)-cyclopropanecarboxylic acid [5-(2-chloro-phenylsulfanyl)-thiazol-2-yl]-amide (50.0 mg, 0.120 mmol) was dissolved in 3 mL of acetic acid containing hydrogen peroxide (30% aqueous solution, 40.8 mg, 0.360 mmol). The mixture was warmed to 85° C. for 1 hour. Ether (1.5 mL) and water (1.5 mL) was added and the layers were separated. the organic layer was dried over sodium sulfate, filtered, and evaporated to dryness. The crude reaction mixture was then separated by reverse-phase preparative liquid chromatography to yield the pure product (19.7 mg, 0.0439 mmol, 36.6%). ESI-MS m/z calc. 448.0. found; 449.1 (M+1)+ Retention time 3.53 minutes. 1H NMR (400 MHz, CD3CN) δ 1.23-1.35 (m, 2H), 1.61-1.68 (m, 2H), 3.80 (s, 3H), 6.90-7.00 (m, 2H), 7.34-7.41 (m, 2H), 7.54-7.68 (m, 3H), 8.03-8.10 (m, 1H), 8.22-8.30 (m, 1H), 9.32 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759335B2
Source datasetuspto-grants-2014_06
ORD IDord-4301237e0320427bbb5e78fde092dd6b
Source noteuspto-grants-2014_06