HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2395944Generated: October 30, 2026
Ethyl isobutyrate → ethyl 4-chloro-2,2-dimethylbutyrate
https://huagongshe.com/reaction/2395944
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl isobutyrate | HCID 7342 | — |
| Reactant | 1-Bromo-2-Chloroethane | HCID 7849 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | ethyl 4-chloro-2,2-dimethylbutyrate | HCID 10797430 | — |
Reaction Steps
To a solution of 22.2 ml of diisopropylamine in 150 ml of tetrahydrofuran being stirred, 93.6 ml of a 1.6 M solution of n-butyl lithium in hexane was added at -5° to 0° C., followed by stirring for 30 minutes. After the reaction mixture was cooled to -78° C. and 19.0 ml of ethyl isobutyrate was added dropwise to the mixture and stirred for 45 minutes. A solution of 11.9 ml of 1-bromo-2-chloroethane in 10 ml of tetrahydrofuran was added dropwise to the reaction mixture. After the reaction mixture was stirred at -78° C. for 1 hour and then at roomtemperature (15° to 20° C.) for 2 hours, an excess amount of an aqueous solution of ammonium chloride was added, followed by extractionwith ethyl acetate. After the extract was washed with water and dried over MgSO4, the solvent was distilled off; the residue was then distilled under reduced pressure, to yield 24.7 g of the title compound in the form of a colorless oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05491145 |
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| Source dataset | uspto-grants-1996_02 |
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| ORD ID | ord-6788a144a8f145d0899ed1b1e9de313d |
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| Source note | uspto-grants-1996_02 |
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