HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 423316Generated: October 30, 2026
Ethanol → Ethyl 4-chloro-3-(trifluoromethyl)benzoate
https://huagongshe.com/reaction/423316
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 4-Chloro-3-(trifluoromethyl)benzoic acid | HCID 2773857 | — |
| Product | Ethyl 4-chloro-3-(trifluoromethyl)benzoate | HCID 46311320 | — |
Reaction Steps
4-Chloro-3-(trifluoromethyl)benzoic acid (1 g, 4.45 mmol) was dissolved in ethanol (3 ml) and concentrated sulfuric acid (0.15 ml) was added. The mixture was heated in the microwave at 100° C. for 5 minutes and then 120° C. for 15 minutes. The solvent was removed in vacuo and the residue partitioned between saturated aq. sodium bicarbonate (50 ml) and ethyl acetate (50 ml). The aqueous layer was extracted with further EtOAc (50 ml) and the organic phases were combined, dried with a phase separator and concentrated in vacuo to give the title compound (1.026 g) (DN108121-148A3) as a colourless oil. δH (methanol-d4, 400 MHz) 1.40 (3H, t), 4.41 (2H, q), 7.76 (1H, d), 8.21 (1H, dd), 8.33 (1H, d). MS (ES) no mass ion observed.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08101775B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-248d688c36c04263bd7aa93ba0bb65da |
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| Source note | uspto-grants-2012_01 |
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