HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248911Generated: October 25, 2026
Potassium Carbonate → HCID 14650107, compound
https://huagongshe.com/reaction/248911
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-bromo-5-(chloromethyl)thiophene | HCID 10198227 | — |
| Reactant | 4-(1-Methyl-1-propyloxy)-phenol | HCID 13882004 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 14650107 | HCID 14650107 | 46.2% |
Reaction Steps
6.64 g of 4-(sec-butyloxy)-phenol and 5.52 g of potassium carbonate are heated in 50 ml of anhydrous dimethylformamide for one hour at 70° C. Subsequently, 8.46 g of 5-bromo-2-chloromethylthiophene in 20 ml anhydrous dimethylformamide is dripped in. The mixture is stirred for 6 hours at 80° C. and overnight at room temperature (about 20° C.). It is then poured into 100 ml of ice water and extracted three times with ethyl acetate, and the organic phases are dried over magnesium sulfate. The solvent is evaporated off to give a crude product which is purified by chromatography on silica gel using n-hexane/ethyl acetate (4:1) as eluant. There is obtained 6.3 g of 2-[4-(sec-butyloxy)-phenoxymethyl]-5-bromothiophene as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05212194 |
|---|
| Source dataset | uspto-grants-1993_05 |
|---|
| ORD ID | ord-5c4afa871395412c8915faf18e66e2f6 |
|---|
| Source note | uspto-grants-1993_05 |
|---|