HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 487891Generated: October 25, 2026
1,4-Naphthalenedicarboxylic acid → 1,4-Naphthalenedimethanol
https://huagongshe.com/reaction/487891
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,4-Naphthalenedicarboxylic acid | HCID 69065 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1,4-Naphthalenedimethanol | HCID 15536753 | 97.8% |
Reaction Steps
A dry 3-neck, 1 L flask equipped with a N2 inlet and dropping funnel is charged with dry THF (200 mL) and LiAlH4 (1.90 g, 0.050 mole). To the stiffed mixture is added via the dropping funnel a hot solution of naphthalene-1,4-dicarboxylic acid (4.32 g, 0.020 mole) in THF (200 mL) over a period of about 1 hour. The resulting mixture is stirred without heating for 90 minutes and then is heated to reflux temperature. After 2 hours, additional LiAlH4 (40 mL of a 1.15 M solution in THF) is added and refluxing continued for 90 minutes. The reaction is stirred at room temperature overnight, then is quenched carefully with THF-water (3:1), acidified to PH <4 with 2N hydrogen chloride, transferred to a separatory funnel and extracted (3 times) with ether. The combined ether extracts are washed with water (2 times), dried (sodium sulfate), filtered, and concentrated to give a white solid (3.68 g). The solid is crystallized from ethyl acetate-hexane, giving (2.68 g) as white crystals, mp 124°-126° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05298498 |
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| Source dataset | uspto-grants-1994_03 |
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| ORD ID | ord-5a430081d2674415a5c542beec1643a4 |
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| Source note | uspto-grants-1994_03 |
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