HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1271712Generated: October 26, 2026
Triethylamine → 4-(2-oxo-2H-pyridin-1-yl)-benzaldehyde
https://huagongshe.com/reaction/1271712
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Sodium Sulfate | HCID 24436 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 18453190 | HCID 18453190 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(2-oxo-2H-pyridin-1-yl)-benzaldehyde | HCID 10703149 | 61% |
Reaction Steps
To a stirred solution of 4-(2-oxo-2H-pyridin-1-yl)-benzoic acid (0.31 g, 1.4 mmol) in THF (12 mL) was added Et3N (0.30 mL, 2.15 mmol, 1.5 eq) followed by dropwise addition of ClCOOEt (0.16 mL, 1.2 eq) at 0° C. under N2. The mixture was stirred for 1 h at 0° C., filtered, and rinsed with THF. The THF solution was stirred at 0° C., MeOH (3 mL) was added followed by portionwise addition of NaBH4 (0.26 g, 6.8 mmol). The mixture was stirred at 0° C. for 20 min, sat'd Na2SO4 added, extracted with CH2Cl2, dried (MgSO4), filtered, and concentrated to dryness to give 4-(2-oxo-2H-pyridin-1-yl)-benzaldehyde (0.17 g) as a tan solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07205318B2 |
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| Source dataset | uspto-grants-2007_04 |
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| ORD ID | ord-404e8cac77324a79bf87521223e5956a |
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| Source note | uspto-grants-2007_04 |
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