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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2405263Generated: October 30, 2026

Diethyl Ether → 3,6-Difluoro-1,2-benzenedimethanol

https://huagongshe.com/reaction/2405263

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantEthyl AcetateHCID 8857—
Reactant3,6-Difluorophthalic anhydrideHCID 513918—
ReactantAluminium lithium hydrideHCID 21226445—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product3,6-Difluoro-1,2-benzenedimethanolHCID 5341432352.1%

Reaction Steps

Lithium aluminium hydride (792 mg, 19.8 mmol) was suspended in THF (6 ml) and cooled in an ice bath. A solution of 4,7-difluoro-isobenzofuran-1,3-dione (730 mg, 3.97 mmol) in THF (6 ml) was added during 5 min. After completion of the reaction (5 min), diethyl ether (30 ml) was added. Subsequently, 2 ml of EA were added in order to decompose excess of lithium aluminium hydride, and thereafter water was slowly added until the alumina salts precipitated. The supernatant was decanted and the precipitate washed twice with EA. The combined extracts were dried over sodium sulfate, filtered and evaporated to dryness to yield 360 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802720B2
Source datasetuspto-grants-2014_08
ORD IDord-89460b7436e44cb9acb76c405aacd345
Source noteuspto-grants-2014_08