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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1672138Generated: October 31, 2026

Ethyl Acetate → HCID 19937311, compound

https://huagongshe.com/reaction/1672138

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant3-(1,3-Dioxo-2,3-dihydro-1H-isoindol-2-yl)-2,2-difluoropropanoic acidHCID 59158333—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 19937311HCID 19937311—

Reaction Steps

Under argon atmosphere 3-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-2,2-difluoro-propionic acid, A2 (13.74 g, 53.85 mmol), dissolved in THF (200 mL) was treated with borane-methylsulfide complex (6.3 mL, 5.04 g, 66.6 mmol). After stirring overnight an additional portion of borane-methylsulfide complex (6.0 mL, 4.80 g, 63.43 mmol) was added. When the reaction was complete it was cautiously diluted with water and extracted with ethyl acetate (2×). An ethyl acetate solution prepared from the residue obtained by evaporation of the initial ethyl acetate extractions at 30° C. in vacuo was washed with water, brine (2×), dried (Na2SO4), filtered, and evaporated in vacuo at 30° C. Crude A3 was sonicated in ethyl acetate, and filtered to give pure 2-(2,2-Difluoro-3-hydroxy-propyl)-isoindole-1,3-dione, A3 (7.45 g). Flash chromatography of the liquor residue (Yamazen, 5 L silica gel cartridge, ethyl acetate/hexane gradient) afforded additional pure 2-(2,2-Difluoro-3-hydroxy-propyl)-isoindole-1,3-dione, A3 (1.39 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07998950B2
Source datasetuspto-grants-2011_08
ORD IDord-6d94f156827b4e99ac64a4e6e303493b
Source noteuspto-grants-2011_08