HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234556Generated: October 30, 2026
Hydrochloric Acid → HCID 131719802, compound
https://huagongshe.com/reaction/234556
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-Fluorophenol | HCID 9732 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | HCID 23354836 | HCID 23354836 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 131719802 | HCID 131719802 | 70.2% |
Reaction Steps
A mixture of 3.58 g of 4-(4-phenyl-4-n-propyl-4-silacyclohexyl)cyclohexanecarboxylic acid, 3.0 g of triphenylphosphine and 50 ml of carbon tetrachloride was agitated under reflux for 6 hours. Then, a mixture of 1.50 g of 4-fluorophenol and 10 ml of pyridine was added to the mixture, followed by further addition of 50 mg of 4-dimethylaminopyridine and agitation at room temperature for 18 hours. The resultant reaction mixture was poured into dilute hydrochloric acid, followed by extraction with ethyl acetate. The ethyl acetate solution was washed with brine, dried and concentrated, followed by purification of the resultant residue with silica gel chromatography to obtain 3.20 g (yield: 70%) of 4-fluorophenyl 4-(4-phenyl-n-propyl-4-silacyclohexyl)cyclohexanecarboxylate. The results of
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05595686 |
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| Source dataset | uspto-grants-1997_01 |
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| ORD ID | ord-c757cfd613114a6dba637692df4b1a13 |
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| Source note | uspto-grants-1997_01 |
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