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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402550Generated: October 27, 2026

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

https://huagongshe.com/reaction/402550

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant2,2-Difluoro-1,3-benzodioxole-5-carboxylic acidHCID 608772—
ReactantRed-AlHCID 16684438—
SolventTolueneHCID 1140—
Product(2,2-Difluoro-1,3-dioxaindan-5-yl)methanolHCID 12814281—

Reaction Conditions

Temperature20 °C

Reaction Steps

Commercially available 2,2-difluoro-1,3-benzodioxole-5-carboxylic acid (1.0 eq) was slurried in toluene (10 vol). Vitride® (2 eq) was added via addition funnel at a rate to maintain the temperature at 15 to 25° C. At the end of the addition, the temperature was increased to 40° C. for 2 hours (h), then 10% (w/w) aqueous (aq) NaOH (4.0 eq) was carefully added via addition funnel, maintaining the temperature at 40 to 50° C. After stirring for an additional 30 minutes (min), the layers were allowed to separate at 40° C. The organic phase was cooled to 20° C., then washed with water (2×1.5 vol), dried (Na2SO4), filtered, and concentrated to afford crude (2,2-difluoro-1,3-benzodioxol-5-yl)-methanol that was used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08742122B2
Source datasetuspto-grants-2014_06
ORD IDord-7160bb79b80e49f78f7766aa234e1ff2
Source noteuspto-grants-2014_06