HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2266565Generated: October 26, 2026
tert-Butanol → 2-(2,4-dichlorobenzyl)-3-oxopentanoic Acid Methyl Ester
https://huagongshe.com/reaction/2266565
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | 2,4-Dichlorobenzyl chloride | HCID 7212 | — |
| Reactant | Methyl 3-oxovalerate | HCID 121699 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(2,4-dichlorobenzyl)-3-oxopentanoic Acid Methyl Ester | HCID 68781491 | — |
Reaction Steps
A suspension of potassium tert-butoxide (8.4 g) in anhydrous tetrahydrofuran (180 mL) at 0° C. was treated with a mixture of tert-butanol (0.4 mL) and 3-oxopentanoic acid methyl ester (9.8 g). After stirring at room temperature for 30 minutes a solution of 2,4-dichloro-1-chloromethylbenzene (14.7 g) in tetrahydrofuran (20 mL) was added and the resulting mixture warmed to room temperature and then stirred at this temperature for 6 days. The mixture was diluted with water (200 mL), extracted with ethyl acetate and the combined extracts washed with water and saturated aqueous sodium chloride solution and then dried over magnesium sulfate. The solvent was removed under reduced pressure and the residue purified by column chromatography on silica gel, eluting with a mixture of pentane and dichloromethane (1:0 to 1:1 by volume) to afford title compound as a white solid, 7.0 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07858640B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-7ba2c4844f9a4e88b3f99dc00193cfaf |
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| Source note | uspto-grants-2010_12 |
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