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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1064834Generated: October 26, 2026

Ammonium Chloride → 3-Methoxymethyloxy-1,2-benzenedimethanol

https://huagongshe.com/reaction/1064834

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantAluminium lithium hydrideHCID 21226445—
Reactant3-Methoxymethyloxyphthalic anhydrideHCID 21936735—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product3-Methoxymethyloxy-1,2-benzenedimethanolHCID 2227285260%

Reaction Steps

After that, lithium aluminum hydride (1.14 g, 30.0 mmol) was added little by little to a solution of 3-methoxymethyloxyphthalic anhydride (3.0 g, 14.4 mmol) in anhydrous tetrahydrofuran (100 ml) under cooling with ice water and the mixture was returned to room temperature followed by stirring for 12 hours. The reaction solution was diluted with ether (300 ml) and a saturated aqueous solution (3 ml) of ammonium chloride was added thereto followed by stirring for 1 hour. The reaction solution was dried over anhydrous magnesium sulfate, filtered off through celite and the filtrate was concentrated to provide 1.71 g (yield 60%) of 3-methoxymethyloxy-1,2-benzenedimethanol as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06969711B2
Source datasetuspto-grants-2005_11
ORD IDord-643fbb12b6c24edf9251de60c65dea63
Source noteuspto-grants-2005_11