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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051844Generated: November 1, 2026

Ammonium Chloride → 3,5-Di(hydroxymethyl)phenol

https://huagongshe.com/reaction/1051844

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant1,3-Benzenedicarboxylic acid, 5-hydroxy-, 1,3-dimethyl esterHCID 83065—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product3,5-Di(hydroxymethyl)phenolHCID 151941582.9%

Reaction Steps

To a solution of dimethyl 5-hydroxyisophthalate (28 g, 133 mmol, 1 eq.) in 1400 mL of dry tetrahydrofuran (THF) at ice-bath temperature, lithium aluminum hydride (LiAlH4 or LAH, 4 eq.) was slowly added with stirring. The resultant mixture was allowed warm to 40° C., stirred at this temperature for 16 hours, and then was added an ammonium chloride (NH4Cl) aqueous solution to quench the reaction. After stirring for 1.5 hours, the mixture was filtered with celite, washed with THF. Organic volatiles were evaporated and the residue was partitioned between water and EtOAc. The aqueous phase was extracted with EtOAc three times. The combined EtOAc layers were dried over MgSO4 to give product (5-hydroxy-1,3-phenylene)dimethanol (17 g, 82%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388193B2
Source datasetuspto-grants-2016_07
ORD IDord-8ab56a45d5df442ab31c34b92e6c53d4
Source noteuspto-grants-2016_07