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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 415682Generated: October 28, 2026

Potassium Carbonate → 3-Benzo[1,3]dioxol-5-yl-5-bromomethyl-[1,2,4]oxadiazole

https://huagongshe.com/reaction/415682

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantBromoacetyl bromideHCID 61147—
ReactantN-Hydroxybenzo[d][1,3]dioxole-5-carboximidamideHCID 178513224—
SolventWaterHCID 962—
Product3-Benzo[1,3]dioxol-5-yl-5-bromomethyl-[1,2,4]oxadiazoleHCID 5940296232.1%

Reaction Conditions

Temperature100 °C

Reaction Steps

Bromoacetyl bromide (0.22 g, 1.10 mmol) was added to N-Hydroxy-benzo[1,3]dioxole-5-carboxamidine (0.40 g, 0.55 mmol) and K2CO3 (0.38 g, 0.78 mmol). The reaction mixture was heated at 100° C. for 15 min. After the completion of the reaction mixture (TLC monitoring), water (25 mL) was added and extracted with ethyl acetate (3×50 mL). The combined organics was washed with water, brine, dried (Na2SO4), filtered and concentrated. The crude residue was purified over silica gel (60-120 M, 5% EtOAc-Hexane) to get the desired product (0.05 g, 31%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088791B2
Source datasetuspto-grants-2012_01
ORD IDord-7dd4de23f2834ae594942ccaaf975e82
Source noteuspto-grants-2012_01