HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1373994Generated: October 26, 2026
Water → 5-Cyclopenten-1-ylpyridine-3-carboxaldehyde
https://huagongshe.com/reaction/1373994
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | N-Formylmorpholine | HCID 20417 | — |
| Reactant | 3-Bromo-5-cyclopenten-1-ylpyridine | HCID 16109521 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 5-Cyclopenten-1-ylpyridine-3-carboxaldehyde | HCID 16109480 | — |
Reaction Steps
A solution of 3-bromo-5-cyclopenten-1-ylpyridine (9) (1 g, 4.5 mmol) in 25 ml of ether is added to a solution of n-butyllithium (1.6M in hexane, 4.2 ml, 6.7 mmol) in 25 ml of ether kept at −60° C. The reaction mixture is stirred for 2 h 30 min at −60° C. and then 1.4 ml of 4-morpholinecarboxaldehyde (13.4 mmol) are added. The reaction is stirred for 1 hour at −60° C. and then poured into water, the organic phase is washed with a saturated aqueous sodium chloride solution, dried over sodium sulfate, filtered and concentrated under reduced pressure. The residue is purified by flash chromatography on silica gel (cyclohexane/ethyl acetate: 80/20). The title product is obtained in the form of a beige solid (0.38 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07163957B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-762401b28d6447b18fb35e53035c8bf9 |
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| Source note | uspto-grants-2007_01 |
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