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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2352572Generated: November 1, 2026

Triethylsilane → Ethyl 4-([1,1'-biphenyl]-4-yl)butanoate

https://huagongshe.com/reaction/2352572

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylsilaneHCID 12052—
ReactantEthyl 4-oxo-4-(4-phenylphenyl)butanoateHCID 12600094—
SolventWaterHCID 962—
SolventTrifluoroacetic acidHCID 6422—
ProductEthyl 4-([1,1'-biphenyl]-4-yl)butanoateHCID 1984345189%

Reaction Steps

Triethylsilane (32.62 ml) was added in one portion to a stirred solution of ethyl 3-(4-phenylbenzoyl)propanoate [(2), 25.06 g] in trifluoroacetic acid (71.5 ml) and the resulting mixture was stirred at room temperature for about 20 hours. The resulting clear dark orange solution was diluted with water and extracted with ether. The extracts were washed with aqueous sodium bicarbonate (x2) and then water (x2), dried and concentrated to give a mobile brown liquid. Triethylsilane remaining in this liquid was removed by Kugelrohr evaporative distillation at 110° C. and a pressure of ca. 1 mmHg to leave crude ethyl 4-(4-phenylphenyl)butanoate (21.20 g) as a brown oil. (Compare method of C. T. West, S. J. Donnelly, D. A. Kooistra and M. P. Doyle, J. Org. Chem., 1973, 38, 2675).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04877811
Source datasetuspto-grants-1989_10
ORD IDord-9ee1429c92e7409bbc4d2a2d32de4ee8
Source noteuspto-grants-1989_10