Water → 4-chloro-7-hydroxy-2H-chromene-3-carbaldehyde
Reaction equation
CN([CH:4]=[O:5])C.O=P(Cl)(Cl)[Cl:8].[Si]([O:28][C:29]1[CH:38]=[C:37]2[C:32]([C:33](=O)[CH2:34][CH2:35][O:36]2)=[CH:31][CH:30]=1)(C(C)(C)C)(C1C=CC=CC=1)C1C=CC=CC=1.O>C(Cl)Cl>[Cl:8][C:33]1[C:32]2[C:37](=[CH:38][C:29]([OH:28])=[CH:30][CH:31]=2)[O:36][CH2:35][C:34]=1[CH:4]=[O:5]Participants
Procedure
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).
Workup
- customSubsequently, to the reaction liquid
- stirringby stirring at room temperature for 1 hour and at 50° C. for 3 hours
- customTo the reaction liquid
- extractionfollowed by extraction with EtOAc twice
- washwashed with water and brine
- dry with materialdried over MgSO4
- concentrationthe liquid was concentrated
- customThe residue was purified by silica gel column chromatography (automatic purification device, hexane:EtOAc=100:0 to 80:20)
Sources & evidence
- ORD record
- ord-bdd8fea4019648fe90581735cfa2ccc8
- Source dataset
- uspto-grants-2012_06
- Patent number
- US08193378B2
Reaction notes
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