HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 589096Generated: October 26, 2026
Hantzsch ester → 2-Pyridin-2-yl-1,2,3,4-tetrahydroquinoline
https://huagongshe.com/reaction/589096
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hantzsch ester | HCID 70849 | — |
| Reactant | 2-Phenylquinoline | HCID 71545 | — |
| Reactant | 2-(2-Pyridinyl)quinoline | HCID 609911 | — |
| Catalyst | Phosphoric acid, diphenyl ester | HCID 13282 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-Pyridin-2-yl-1,2,3,4-tetrahydroquinoline | HCID 90409822 | 94% |
Reaction Steps
A suspension of 2-pyridin-2-ylquinoline (0.767 g, 3.72 mmol), 1,4-dihydro-3,5-dicarbethoxy-2,6-dimethylpyridine (2.17 g, 8.55 mmol), and diphenyl hydrogen phosphate (0.0093 g, 0.037 mmol) in benzene (18.6 mL) was heated at 60° C. for 10 h. The reaction mixture was treated with 2-phenylquinoline (0.305 g, 1.49 mmol) and heated at 60° C. for 3 h. The reaction mixture was then concentrated to a crude solid. Purification by flash column chromatography (100% hexanes to 50% ethyl acetate/hexanes [the ethyl acetate contained 5% methanol]) gave the desired product (0.735 g, 94%) as a racemic mixture. LCMS calculated for C14H15N2 (M+H)+: m/z=211.1. found: 211.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09227985B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-7a113bd58e384bfeb7125394694985eb |
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| Source note | uspto-grants-2016_01 |
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