HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827944Generated: October 27, 2026
Ethanol → 2-Phenyl-1,2,3,4-tetrahydroquinoline
https://huagongshe.com/reaction/1827944
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | 2-Phenylquinoline | HCID 71545 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Phenyl-1,2,3,4-tetrahydroquinoline | HCID 10752915 | — |
Reaction Steps
In Scheme A, step 2, the 2-phenyl-1,2,3,4-tetrahydroquinoline of formula (3) is prepared by reducing 2-phenylquinoline of formula (2). For example, 2-phenylquinoline of formula (2) is dissolved in a suitable alcoholic solvent, such as absolute ethanol. Sodium metal is then added and the reaction is allowed to cool to room temperature. The reaction mixture may then be diluted with water and extracted with a suitable organic solvent, such as methylene chloride, ethyl acetate, or chloroform. The combined extracts may then be washed with water and brine, the organic layer is separated and dried and the solvent is evaporated in vacuo to provide the 2-phenyl-1,2,3,4-tetrahydroquinoline of formula (3) which may be used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07056931B2 |
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| Source dataset | uspto-grants-2006_06 |
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| ORD ID | ord-4c618bcdc1b04c0690100d32180e82aa |
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| Source note | uspto-grants-2006_06 |
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