HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 426604Generated: October 29, 2026
3-(Trifluoromethyl)phenol → Ethyl 2-[3-(trifluoromethyl)phenoxy]acetate
https://huagongshe.com/reaction/426604
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-(Trifluoromethyl)phenol | HCID 7376 | — |
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Ethyl 2-[3-(trifluoromethyl)phenoxy]acetate | HCID 4507464 | 80.8% |
Reaction Steps
A mixture of 100 g (0.618 mole) of α,α,α-trifluoro-m-cresol, 106 g (0.632 mole) of ethyl bromoacetate, 87.5 g (0.632 mole) of potassium carbonate, and 1500 ml of acetone is stirred at reflux for 4 hours, and at room temperature for 18 hours. The mixture is filtered, evaporated under vacuum on a rotorary evaporator at 45° C. and at 85° C. (0.1 mm) to remove excess ethyl bromoacetate. The reaction mixture is taken up in 500 ml of ether, washed three times with 100 ml each of 0.1 M potassium carbonate, once with 100 ml of water, 100 ml of 0.01 M hydrochloric acid, and 100 ml of water. It is then dried with magnesium sulfate, filtered and evaporated, giving 142 g of the crude product. This is fractionally distilled at 73°-75° C. (0.1 mm) to give 124 g of the purified subject product as a colorless liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04170597 |
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| Source dataset | uspto-grants-1979_10 |
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| ORD ID | ord-c939e30221ac4010acbdb273ecdad22c |
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| Source note | uspto-grants-1979_10 |
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