HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1896764Generated: October 31, 2026
Triethylamine → 2-(4-Chlorobenzylthio)-5-nitrobenzo[d]oxazole
https://huagongshe.com/reaction/1896764
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-(Bromomethyl)-4-chlorobenzene | HCID 69329 | — |
| Reactant | 5-Nitrobenzo[D]Oxazole-2-Thiol | HCID 786293 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-(4-Chlorobenzylthio)-5-nitrobenzo[d]oxazole | HCID 67332584 | 78% |
Reaction Steps
To a suspension of 5-nitrobenzo[d]oxazole-2(3H)-thione (196.2 mg, 1.0 mmol) in chloroform (10 mL) was added triethylamine (278 μL, 2 mmol) followed by 1-(bromomethyl)-4-chlorobenzene (226 mg, 1.1 mmol). The reaction was stirred at 60° C. for 2 h. After cooling, the reaction was diluted with ethyl acetate, washed with dilute aqueous hydrochloric solution and brine. The combined organic layers were dried over anhydrous MgSO4 and evaporated. The resulting solid was purified by column chromatography eluting with ethyl acetate/hexanes 1:10 v/v to afford 250 mg (78%) of the title compound (LCMS RT=7.64 min)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08518980B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-f8a300d4dc894f7ab4a38ff306059c8e |
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| Source note | uspto-grants-2013_08 |
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