HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 885077Generated: October 31, 2026
Trifluoroacetic acid → Trifluoroacetic acid
https://huagongshe.com/reaction/885077
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 58026046 | HCID 58026046 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Trifluoroacetic acid | HCID 6422 | 100% |
| Product | HCID 58026061 | HCID 58026061 | — |
Reaction Steps
To a solution of 2-benzyl-5-phenyl-1,2,3,4-tetrahydro-2,6-naphthyridine, 2 TFA (0.48 g, 0.908 mmol) in MeOH (10 mL) was added Pd/C (0.193 g, 0.182 mmol). The mixture was flushed with N2, then was purged with H2 and stirred at rt under 1 atm. After stirring the reaction for 3 h it was filtered through a pad of CELITE®. The organic solution was concentrated under reduced pressure to give 5-phenyl-1,2,3,4-tetrahydro-2,6-naphthyridine, 2 TFA (0.398 g, 0.908 mmol, 100% yield) as a light-brown oil which crystallized under vacuum. The residue was used in the next step with no additional purification. LC/MS: m/z 211.00 (M+H)+, 0.270 min (method 7). 1H NMR (500 MHz, MeOD) δ ppm 8.66 (d, 1H) 7.74 (d, J=5.49 Hz, 1H) 7.57-7.67 (m, 5H) 4.69 (s, 2H) 3.54 (t, J=6.10 Hz, 2H) 3.11 (t, J=6.10 Hz, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08242124B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-fdbdcee348d442a790aeafeae3bd10c5 |
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| Source note | uspto-grants-2012_08 |
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