HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2371098Generated: October 30, 2026
Hydrochloric Acid → Tert-butyl 5-biphenyl-4-yl-3-oxopentanoate
https://huagongshe.com/reaction/2371098
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tert-butyl acetoacetate | HCID 15538 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1,1'-Biphenyl, 4-(bromomethyl)- | HCID 257716 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Tert-butyl 5-biphenyl-4-yl-3-oxopentanoate | HCID 58914664 | 50.8% |
Reaction Steps
A solution of tert-butyl acetoacetate (7.2 g) in tetrahydrofuran (80 ml) was added to a stirred solution of sodium hydride (1.33 g) in tetrahydrofuran (60 ml) at 0° C. under nitrogen atmosphere. The reaction mixture was stirred for 10 minutes followed by the addition of n-butyl lithium (23 ml, 2.5 M solution in hexane) dropwise over 10 minutes. The resulting reaction mixture was stirred for 10 minutes. A solution of 4-(bromomethyl) biphenyl (12.5 g) in tetrahydrofuran (60 ml) was added over 10 minutes and the resulting solution was stirred at 0° C. for approximately 2 hours. To resulting mixture was added hydrochloric acid (6 M, 15 ml) followed by extracting the mixture with diethyl ether. The organic layers were combined, washed with water and brine and dried over anhydrous sodium sulphate. The solvent was evaporated under reduced pressure and the residue thus obtained was purified by silica gel column chromatography using 8% ethyl acetate-hexane as eluant to furnish the title compound (7.5 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08710261B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-20ee7ed2e6d4424fb351a213790e2d5b |
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| Source note | uspto-grants-2014_04 |
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