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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Reactant | N-Hydroxybenzo[d][1,3]dioxole-5-carboximidamide | HCID 178513224 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Benzo[1,3]dioxol-5-yl-5-bromomethyl-[1,2,4]oxadiazole | HCID 59402962 | 32.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08088791B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-7dd4de23f2834ae594942ccaaf975e82 |
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| Source note | uspto-grants-2012_01 |
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