HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 381819Generated: October 25, 2026
4-Fluorobiphenyl → Methyl 4-(4'-fluoro-4-biphenylyl)-4-oxo-butyrate
https://huagongshe.com/reaction/381819
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Fluorobiphenyl | HCID 9461 | — |
| Reactant | Butanoic acid, 4-chloro-4-oxo-, methyl ester | HCID 73888 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 4-(4'-fluoro-4-biphenylyl)-4-oxo-butyrate | HCID 15541120 | 74.6% |
Reaction Steps
To a stirred suspension of anhydrous aluminum chloride (9.64 g, 0.723 mol) in dichloromethane (90 mL) at 5° C. was added dropwise a solution of 4-fluorobiphenyl (4.97 g, 0.0289 mol) in dichloromethane (40 mL) followed by the dropwise addition of a solution of 3-carbomethoxypropionyl chloride (3.94 mL, 0.032 mol) in dichloromethane (30 mL), and the mixture stirred. After 2 hours at 5° C., the mixture was allowed to warm to room temperature. After 1 day, the reaction was cooled to 5° C. and quenched by the dropwise addition of water (160 mL). The layers were separated, and the organic layer washed with brine, dried (Na2SO4), and rotary evaporated. The residue was recrystallized from methanol (300 mL) to give 6.17 g of 4-(4′-fluoro-biphenyl-4-yl)-4-oxo-butyric acid, methyl ester as a pale yellow solid; mp 131.5-133.0° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06307089B2 |
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| Source dataset | uspto-grants-2001_10 |
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| ORD ID | ord-e554754d25da4b91b1ad3a91d61b2761 |
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| Source note | uspto-grants-2001_10 |
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