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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | Ethyl 4-oxo-4-(4-phenylphenyl)butanoate | HCID 12600094 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | Ethyl 4-([1,1'-biphenyl]-4-yl)butanoate | HCID 19843451 | 89% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04877811 |
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| Source dataset | uspto-grants-1989_10 |
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| ORD ID | ord-9ee1429c92e7409bbc4d2a2d32de4ee8 |
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| Source note | uspto-grants-1989_10 |
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