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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1665721Generated: October 28, 2026

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

https://huagongshe.com/reaction/1665721

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/E.A.=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, 1 H), 7.26 (dd, J=1.5, 9.3 Hz, 1 H), 7.19 (d, J=1.2 Hz, 1 H), 6.16 (s, 2 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08039491B2
Source datasetuspto-grants-2011_10
ORD IDord-bddb95a2d510462eb3c5fd7a38a87e56
Source noteuspto-grants-2011_10