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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTert-butyl acetoacetateHCID 15538—
ReactantSodium hydrideHCID 24758—
Reactant1,1'-Biphenyl, 4-(bromomethyl)-HCID 257716—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 5-biphenyl-4-yl-3-oxopentanoateHCID 5891466450.8%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710261B2
Source datasetuspto-grants-2014_04
ORD IDord-20ee7ed2e6d4424fb351a213790e2d5b
Source noteuspto-grants-2014_04