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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 7-{[tert-butyl(diphenyl)silyl]oxy}-2,3-dihydro-4H-chromen-4-one | HCID 58438647 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-chloro-7-hydroxy-2H-chromene-3-carbaldehyde | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08193378B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-bdd8fea4019648fe90581735cfa2ccc8 |
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| Source note | uspto-grants-2012_06 |
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