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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1847310Generated: October 24, 2026

Water → 6-Fluoro-1,3-dioxaindane-5-carbaldehyde

https://huagongshe.com/en/reaction/1847310

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCesium carbonateHCID 10796—
Reactant2-Fluoro-4,5-dihydroxybenzaldehydeHCID 593363—
SolventDimethylformamideHCID 6228—
Product6-Fluoro-1,3-dioxaindane-5-carbaldehydeHCID 1438444324%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a stirred solution of 2-fluoro-4,5-dihydroxy-benzaldehyde (8.0 g) and BrClCH2 (24.8 g, 190 mmol) in dry DMF (50 mL) was added Cs2CO3 (62.0 g, 190 mmol) in portions. The resulting mixture was stirred at 60° C. overnight and then poured into water. The mixture was extracted with EtOAc (200 mL×3). The combined organic layers were washed with brine (200 mL), dried over Na2SO4, and evaporated in vacuo to give crude product, which was purified by column chromatography on silica gel (5-20% ethyl acetate/petroleum ether) to afford 6-fluoro-benzo[1,3]dioxole-5-carbaldehyde (700 mg, two steps yield: 24%). 1H-NMR (400 MHz, CDCl3) δ 10.19 (s, 1H), 7.23 (d, J=5.6, 1H), 6.63 (d, J=9.6, 1H), 6.08 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952050B2
Source datasetuspto-grants-2015_02
ORD IDord-0d81e20bba2a425d986c6284e91fd468
Source noteuspto-grants-2015_02