HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 257757Generated: October 26, 2026
Potassium Carbonate → 2-[4-(6-Chloro-2-pyridinyloxy)-phenoxymethyl]-5-bromothiophene
https://huagongshe.com/reaction/257757
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Bromo-5-(chloromethyl)thiophene | HCID 10198227 | — |
| Reactant | 4-(6-Chloro-2-pyridinyloxy)phenol | HCID 14673606 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-[4-(6-Chloro-2-pyridinyloxy)-phenoxymethyl]-5-bromothiophene | HCID 14673607 | 49.5% |
Reaction Steps
3.5 g of 4-(6-chloro-2-pyridinyloxy)-phenol and 3.2 g of potassium carbonate are stirred for one hour at 60° C. in 100 ml of anhydrous dimethylformamide. Subsequently, 6.5 g of 5-bromo-2-chloromethylthiophene in 30 ml of anhydrous dimethylformamide is dripped in. The mixture is stirred for 6 hours at 80° C. and overnight at room temperature (about 20° C.). The mixture is then poured into 200 ml of ice water. The crude product which precipitates out is filtered off and recrystallized from n-hexane/ethyl acetate (4/1). There is obtained 3.1 g of 2-[4-(6-chloro-2-pyridinyloxy)-phenoxymethyl]-5-bromothiophene of m.p.: 78°-80° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05264434 |
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| Source dataset | uspto-grants-1993_11 |
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| ORD ID | ord-d992e207548b486ca0ceeedeca087612 |
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| Source note | uspto-grants-1993_11 |
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