HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1598503Generated: November 2, 2026
Diethyl Carbonate → Ethyl 2,6-dichloro-4-(trifluoromethyl)benzoate
https://huagongshe.com/reaction/1598503
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Carbonate | HCID 7766 | — |
| Reactant | 4-Bromo-3,5-dichlorobenzotrifluoride | HCID 1268256 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Ethyl 2,6-dichloro-4-(trifluoromethyl)benzoate | HCID 54315306 | — |
Reaction Steps
To a mixture of 65.2 ml of n-butyllithium (1.61M in hexane) and 100 ml of anhydrous ether was added dropwise 29.3 g of 4-bromo-3,5-dichlorobenzo-trifluoride (3) in 30 ml of anhydrous ether at -78° C., followed by stirring for 20 minutes. Subsequently, 13.3 ml of diethyl carbonate in 50 ml of anhydrous ether was added dropwise to the mixture, followed by stirring at -78° C. for 30 minutes and then at 0° C. for 30 minutes. Ice water was added to the reaction mixture, the mixture was extracted with ether, and the combined ethereal layer was washed with brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The resulting residue was distilled under reduced pressure, giving 18.3 g of the desired product in the form of a colorless oil (yield 63.8%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05739083 |
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| Source dataset | uspto-grants-1998_04 |
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| ORD ID | ord-c728241423534602a7198901d3a87cc3 |
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| Source note | uspto-grants-1998_04 |
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