Back
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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-Naphthalenedicarboxylic acidHCID 69065—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product1,4-NaphthalenedimethanolHCID 1553675397.8%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05298498
Source datasetuspto-grants-1994_03
ORD IDord-5a430081d2674415a5c542beec1643a4
Source noteuspto-grants-1994_03