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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217424Generated: October 30, 2026

Water → 4-chloro-7-hydroxy-2H-chromene-3-carbaldehyde

https://huagongshe.com/reaction/217424

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDimethylformamideHCID 6228—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant7-{[tert-butyl(diphenyl)silyl]oxy}-2,3-dihydro-4H-chromen-4-oneHCID 58438647—
SolventDichloromethaneHCID 6344—
Product4-chloro-7-hydroxy-2H-chromene-3-carbaldehydeHCID 58438709—

Reaction Steps

To a solution of DMF (2 mL) in DCM (7.5 mL) was added dropwise POCl3 (1.39 mL) at 0° C., followed by stirring at room temperature for 30 minutes. Subsequently, to the reaction liquid was added dropwise a solution of 7-{[tert-butyl(diphenyl)silyl]oxy}-2,3-dihydro-4H-chromen-4-one (2.00 g) in DCM (11 mL), followed by stirring at room temperature for 1 hour and at 50° C. for 3 hours. To the reaction liquid was added water, followed by extraction with EtOAc twice. The organic layer was combined, washed with water and brine, and dried over MgSO4, and the liquid was concentrated. The residue was purified by silica gel column chromatography (automatic purification device, hexane:EtOAc=100:0 to 80:20) to obtain 4-chloro-7-hydroxy-2H-chromene-3-carbaldehyde (720 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193378B2
Source datasetuspto-grants-2012_06
ORD IDord-bdd8fea4019648fe90581735cfa2ccc8
Source noteuspto-grants-2012_06