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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1509315Generated: November 1, 2026

Hydrogen Peroxide → 1-(4-Bromophenyl)-3,3-dimethoxycyclobutanecarboxamide

https://huagongshe.com/reaction/1509315

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(4-Bromophenyl)-3,3-dimethoxycyclobutanecarbonitrileHCID 59487135—
SolventDimethyl SulfoxideHCID 679—
Product1-(4-Bromophenyl)-3,3-dimethoxycyclobutanecarboxamideHCID 67254266488.5%

Reaction Steps

Hydrogen peroxide (2.05 ml, 20.07 mmol) was added over 2 h to a stirred mixture of 1-(4-bromophenyl)-3,3-dimethoxycyclobutanecarbonitrile (3.18 g, 10.74 mmol) and Potassium carbonate (0.297 g, 2.15 mmol) in DMSO (11 ml) at 40 degree under a nitrogen atmosphere. After the addition, the reaction mixture was heated to 80 degree for 3 h. The reaction mixture was allowed to cool down to room temperature and water (30 ml) was added. The reaction mixture was extracted with ethyl acetate (3×20 ml). The combined organic phase was washed with water (2×30 ml), brine (30 ml), concentrated to give light yellow oil (3.3 g). 1H NMR (500 MHz, CDCl3) 7.40 (d, 2H), 7.11 (d, 2H), 5.89 (br, 1H), 5.58 (br, 1H), 3.12 (s, 3H), 3.02 (s, 3H), 2.97 (d, 2H), 2.52 (d, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221838B2
Source datasetuspto-grants-2015_12
ORD IDord-a8d906d6df8446caa0da94adeb381cd2
Source noteuspto-grants-2015_12