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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1728189Generated: October 27, 2026

Naphthalene → 5-Chloro-pyridine-3-carbaldehyde

https://huagongshe.com/reaction/1728189

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNaphthaleneHCID 931—
ReactantSulfurHCID 5362487—
Reactant3-chloro-5-formyl-2H-pyridine-1-carboxylic acid phenyl esterHCID 57565931—
SolventDiethyl EtherHCID 3283—
Product5-Chloro-pyridine-3-carbaldehydeHCID 14444196—

Reaction Steps

The mixture of 3-chloro-5-formyl-2H-pyridine-1-carboxylic acid phenyl ester (2.3 g, 8.8 mmol), sublimed sulfur (0.29 g, 9 mmol) and naphthalene (6 g) was refluxed under an argon atmosphere for 2 h. After the reaction was complete, the mixture was cooled to r.t., dissolved in ethyl ether (30 mL), and extracted with aqueous 10% HCl. The combined acid extracts were washed with ethyl ether (20 mL) and cooled to 0° C. Dichloromethane (30 mL) was added and “pH” of the mixture was adjusted to be basic with 25% aqueous NaOH, and the mixture was extracted with dichloromethane (20 mL). The combined organic phase was washed with brine, dried over K2CO3, filtered, and concentrated to give a brown solid. (0.8 g, 76%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07495007B2
Source datasetuspto-grants-2009_02
ORD IDord-58e86f768a244136a67dc6224cf5b5d3
Source noteuspto-grants-2009_02