HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 465438Generated: October 31, 2026
Hydrochloric Acid → Ethyl 3-(4-acetonylphenyl)-2-chloropropionate
https://huagongshe.com/reaction/465438
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl 2-chloroacetoacetate | HCID 11858 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-(4-(Bromomethyl)phenyl)propan-2-one | HCID 19874489 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 3-(4-acetonylphenyl)-2-chloropropionate | HCID 19874575 | — |
Reaction Steps
A solution of ethyl 2-chloroacetoacetate (8.25 g) in dry dimethylformamide was treated with sodium hydride (1.3 g and stirred at ambient temperature for 0.5 h. A solution of 4-(bromomethyl)phenylpropan-2-one, ethylene ketal (12.0 g) in dry dimethylformamide (20 ml) was then added and the mixture was heated at 70° C. for 4 h. The reaction mixture was cooled, poured into ice/water, acidified with 2N-hydrochloric acid, extracted with ethyl acetate (4×50 ml) and the combined organic extracts dried (magnesium sulphate), filtered and evaporated in vacuo. The residue was dissolved in ethanol and treated at 0°-5° C. with barium hydroxide hydrate (7.7 g). The mixture was stirred for 0.5 h, poured into ice/water, extracted with ethyl acetate (3×50 ml) and the combined organic extracts dried (magnesium sulphate), filtered and evaporated in vacuo to leave a red oil, which was purified by column chromatography on silica using diethyl ether: petroleum ether (60°-80°) (30:70) as eluent to give ethyl 3-(4-acetonylphenyl)-2-chloropropionate, ethylene ketal, (6.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05153210 |
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| Source dataset | uspto-grants-1992_10 |
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| ORD ID | ord-be8b5aa939354b438e2ad3827832cb73 |
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| Source note | uspto-grants-1992_10 |
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