HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1623734Generated: October 27, 2026
Potassium Carbonate → Methyl 2-{[(4-fluorophenyl)methyl]oxy}-5-{1-[2-(methyloxy)ethyl]-1H-pyrazol-4-yl}benzoate
https://huagongshe.com/reaction/1623734
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Bromoethyl methyl ether | HCID 80972 | — |
| Reactant | Methyl 2-{[(4-fluorophenyl)methyl]oxy}-5-(1H-pyrazol-4-yl)benzoate | HCID 67107242 | — |
| Product | Methyl 2-{[(4-fluorophenyl)methyl]oxy}-5-{1-[2-(methyloxy)ethyl]-1H-pyrazol-4-yl}benzoate | HCID 67108000 | — |
Reaction Steps
To a solution of methyl 2-{[(4-fluorophenyl)methyl]oxy}-5-(1H-pyrazol-4-yl)benzoate (may be prepared as described in Description 115; 200 mg, 0.61 mmol) was added 2-bromoethyl methyl ether (0.10 ml, 1.23 mmol), potassium carbonate (254 mg, 1.84 mmol) and the reaction mixture was stirred at room temperature. The reaction mixture was then warmed to 50° C. for 5 hours. The reaction was filtered to remove the potassium carbonate, and the organics were evaporated on a buchi under reduced pressure. The solid was taken up into ethyl acetate (50 ml) and this was washed with water (1×25 ml). The organics were dried (MgSO4) and evaporated under reduced pressure on a buchi to yield the title compound. The crude product was used directly without further purification. 240 mg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08778939B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-3b795812e2224438afebcdd336239cc7 |
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| Source note | uspto-grants-2014_07 |
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