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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1581448Generated: November 2, 2026

HCID 23530181, compound → 2,6-Naphthalenedicarboxylic acid

https://huagongshe.com/reaction/1581448

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 23530181HCID 23530181—
SolventDichloromethaneHCID 6344—
Product2,6-Naphthalenedicarboxylic acidHCID 14357—
ProductHCID 23530181HCID 23530181—

Reaction Steps

2.6 Grams (10.3 mmol) of (R)-4-hydroxy-1-(3-ethyl-1-methylpentyloxycarbonyl)benzene obtained in the same manner as in (3) of Example 4, 1.0 g (4.92 mmol) of 2,6-naphthalenedicarboxylic acid and 50 ml of dehydrated dichloromethane were placed in a reactor, 2.3 g (11.1 mmol) of dicyclohexylcarbodiimide and 0.26 g (2.1 mmol) of 4-dimethylaminopyridine were added, and the mixture was stirred at room temperature for 24 hours. To the reaction solution was added 20 ml of water, and the mixture was stirred at room temperature for 1 hour. Then, the reaction mixture was filtered with Celite, and diethyl ether was added to separate a liquid of an organic layer. The organic layer was washed with 2N hydrochloric acid, washed with a 1N sodium hydroxide aqueous solution and then washed with water. The washed organic layer was dried over anhydrous sodium sulfate and filtered, and the solvent was distilled off. The thus-obtained crude product was purified by silica gel chromatography, to give 2.0 g (2.93 mmol, yield 59%) of an end compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06730371B2
Source datasetuspto-grants-2004_05
ORD IDord-96846533ed2b46dcaa3bf13c4ba8c850
Source noteuspto-grants-2004_05