HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383534Generated: October 25, 2026
Hydrochloric Acid → 4-Nitro-3-trifluoromethyl-phenoxyethyl acetate
https://huagongshe.com/reaction/383534
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-Nitro-3-trifluoromethylphenol | HCID 6931 | — |
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4-Nitro-3-trifluoromethyl-phenoxyethyl acetate | HCID 67520014 | 114.4% |
Reaction Steps
Ethyl bromoacetate (1.2 g, 10.9 mmol) was added in the suspension of 4-nitro-3-trifluoromethyl phenol (2.0 g, 9.66 mmol) and potassium carbonate (2.0 g, 14.5 mmol) in acetone, and the mixture was attired at room temperature for 6 hours. After the reaction mixture had been poured in ice water and acidified with 2N hydrochloric acid, the mixture was extracted with ethyl acetate. The organic layer was washed with 5% sodium hydrogencarbonate aqueous solution and then with water, and dried with anhydrous sodium sulfate. The solvent was removed by distillation under reduced pressure, and 4-nitro-3-trifluoromethyl-phenoxyethyl acetate (3.24 g (theoretical amount: 2.83 g), 100%) was obtained as a yellow solid and was used in the next reaction without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08367666B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-ddfbbc03f67d4b479bc0597f136195a4 |
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| Source note | uspto-grants-2013_02 |
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