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
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 23530181 | HCID 23530181 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,6-Naphthalenedicarboxylic acid | HCID 14357 | — |
| Product | HCID 23530181 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06730371B2 |
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| Source dataset | uspto-grants-2004_05 |
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| ORD ID | ord-96846533ed2b46dcaa3bf13c4ba8c850 |
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| Source note | uspto-grants-2004_05 |
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