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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767766Generated: October 26, 2026

Water → 5-Cyclopenten-1-ylpyridine-3-carboxaldehyde

https://huagongshe.com/reaction/1767766

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantN-FormylmorpholineHCID 20417—
Reactant3-Bromo-5-cyclopenten-1-ylpyridineHCID 16109521—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
Product5-Cyclopenten-1-ylpyridine-3-carboxaldehydeHCID 16109480—

Reaction Conditions

Temperature-60 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07235568B2
Source datasetuspto-grants-2007_06
ORD IDord-b5437d123c6a4b43afb5d421c0b06394
Source noteuspto-grants-2007_06