HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2296048Generated: October 31, 2026
Ethyl isobutyrate → 2,2-Dimethyl-3-[4-(3-pyridylmethyl)phenyl]propionic acid ethyl ester
https://huagongshe.com/reaction/2296048
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl isobutyrate | HCID 7342 | — |
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Solvent | Hexamethylphosphoramide | HCID 12679 | — |
| Product | 2,2-Dimethyl-3-[4-(3-pyridylmethyl)phenyl]propionic acid ethyl ester | HCID 54391330 | — |
Reaction Steps
To a 3.0 M solution of lithium diisopropylamide in tetrahydrofuran [prepared from diisopropylamine (0.56 ml), tetrahydrofuran (5 ml) and a 1.4 M solution of butyllithium in hexane (2.2 ml)] was added dropwise 0.41 ml of ethyl isobutyrate at -70° C., and the mixture was stirred at that temperature for 40 minutes. To it was added dropwise a solution of 0.26 g of the benzyl chloride compound (prepared as described in Reference Example 2) in 2.8 ml of a mixture of HMPA and tetrahydrofuran (1:1) at -70° C., and the mixture was stirred at that temperature for 2 hours, and then at room temperature for one hour. The reaction mixture was poured into a saturated aqueous solution of ammonium chloride, and extracted with diethyl ether. The extract was washed with a saturated aqueous solution of sodium chloride, dried over sodium sulphate and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel using a mixture of cyclohexane and ethyl acetate (2:1) as eluent to give 0.27 g of the title compound having the following physical characteristics:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04427682 |
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| Source dataset | uspto-grants-1984_01 |
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| ORD ID | ord-4f0835d2082d400bb8604b3dae8f1693 |
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| Source note | uspto-grants-1984_01 |
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