HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 80417Generated: October 29, 2026
Benzyl Bromide → 2-(Benzylthio)-5-phenyl-1,3,4-oxadiazole
https://huagongshe.com/reaction/80417
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 178527944 | HCID 178527944 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(Benzylthio)-5-phenyl-1,3,4-oxadiazole | HCID 2843335 | — |
Reaction Steps
A suspension of 5-phenyl-[1,3,4]oxadiazole-2-thiol (3.1 g, 17.4 mmol; Aldrich) in ethanol (30 mL) was cooled to 0° C. and treated with diisopropylethylamine (3.1 mL, 17.4 mmol; Aldrich). The suspension cleared. Benzyl bromide (2.08 mL, 17.4 mmol; Aldrich) was then added, and the mixture was allowed to warm to room temperature. After 45 minutes, the resulting precipitate was collected by filtration and dried to afford the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846661B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-612e26202f5b4b5f849e68095060fd5e |
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| Source note | uspto-grants-2014_09 |
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