HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1820853Generated: October 26, 2026
Hydrochloric Acid → Ethyl 3-(4'-chlorobiphenyl-4-yl)-3-oxopropionate
https://huagongshe.com/reaction/1820853
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Propanedioic acid, monoethyl ester | HCID 3595298 | — |
| Reactant | 4'-Chlorobiphenyl-4-carbonyl chloride | HCID 9834814 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 3-(4'-chlorobiphenyl-4-yl)-3-oxopropionate | HCID 57892092 | — |
Reaction Steps
4.29 g (32.5 mmol) of monoethyl malonate is dissolved in 100 mL of THF and 42.3 mL (67.7 mmol) of butyllithium solution (1.6N in hexane) is added dropwise at −60° C. The temperature is allowed to come up to −15° C., then the mixture is cooled again to −65° C. and 3.40 g (13.5 mmol) of 4′-chlorobiphenyl-4-carboxylic acid chloride (for preparation see Gazz. Chim. Ital. 1949, 79, 453.) in 30 mL of THF is added dropwise. The mixture is kept for 5 minutes at −65° C., then heated for 2 hours to ambient temperature. The mixture is poured onto 50 mL of 1N hydrochloric acid, extracted with 300 mL of diethyl ether, and the organic phase is washed with saturated sodium hydrogen carbonate solution and water and finally dried over sodium sulfate. The solvent is eliminated, the residue is recrystallized from petroleum ether and the product is dried in vacuo. Yield: 3.10 g (76% of theory); Rf value: 0.60 (silica gel, petroleum ether/ethyl acetate=5:2); m.p. 45° C.-50° C.; C17H15ClO3; EII mass spectrum: m/z=303/305 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07605176B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-2c4460cc02c148a684aa9d853e8dc740 |
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| Source note | uspto-grants-2009_10 |
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