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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1908364Generated: October 28, 2026

Water → 7-Fluorobenzo[d][1,3]dioxole-5-carbaldehyde

https://huagongshe.com/reaction/1908364

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCesium carbonateHCID 10796—
Reactant3-Fluoro-4,5-dihydroxybenzaldehydeHCID 593664—
SolventDimethylformamideHCID 6228—
Product7-Fluorobenzo[d][1,3]dioxole-5-carbaldehydeHCID 5912915349.6%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 3-fluoro-4,5-dihydroxy-benzaldehyde (1.5 g, 9.6 mmol) and BrClCH2 (4.9 g, 38.5 mmol) in dry DMF (50 mL) was added Cs2CO3 (12.6 g, 39 mmol). The mixture was stirred at 60° C. overnight and was then poured into water. The resulting mixture was extracted with EtOAc (50 mL×3). The combined organic layers were washed with brine (100 mL), dried over Na2SO4 and evaporated under reduced pressure to give the crude product, which was purified by column chromatography on silica gel (petroleum ether/ethyl acetate=10/1) to afford 7-fluoro-benzo[1,3]dioxole-5-carbaldehyde (0.80 g, 49%). 1H NMR (300 MHz, CDCl3) δ 9.78 (d, J=0.9 Hz, 1H), 7.26 (dd, J=1.5, 9.3 Hz, 1H), 7.19 (d, J=1.2 Hz, 1H), 6.16 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598181B2
Source datasetuspto-grants-2013_12
ORD IDord-3e0dbafbfc9b4a70a449c8cff20d3bc4
Source noteuspto-grants-2013_12