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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1673123Generated: November 2, 2026

Water → (2,2-Difluoro-1,3-dioxaindan-5-yl)methanol

https://huagongshe.com/reaction/1673123

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantAluminium lithium hydrideHCID 21226445—
Reactant1,3-Benzodioxole-5-carboxylic acid, 2,2-difluoro-, methyl esterHCID 59129261—
SolventTetrahydrofuranHCID 8028—
Product(2,2-Difluoro-1,3-dioxaindan-5-yl)methanolHCID 12814281—

Reaction Steps

Methyl 2,2-difluorobenzo[d][1,3]dioxole-5-carboxylate from previous step (11.5 g) dissolved in anhydrous tetrahydrofuran (20 mL) was slowly added to a suspension of lithium aluminum hydride (4.10 g, 106 mmol) in anhydrous THF (100 mL) at 0° C. The mixture was then warmed to room temperature and stirred at for 1 h. The reaction mixture was cooled to 0° C. and treated with water (4.1 g), followed by sodium hydroxide (10% aqueous solution, 4.1 mL). The resulting slurry was filtered and washed with THF. The combined filtrate was evaporated to dryness and the residue was purified by silica gel column chromatography to give (2,2-difluorobenzo[d][1,3]dioxol-5-yl)methanol as a colorless oil (7.2 g, 76% over two steps).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07999113B2
Source datasetuspto-grants-2011_08
ORD IDord-2528a5684b18484da1e1f3950c4301c9
Source noteuspto-grants-2011_08