Dimethylformamide → HCID 86647905, compound
Reaction equation
CN(C)[CH:3]=[O:4].O=P(Cl)(Cl)[Cl:8].[CH3:11][O:12][C:13]1([CH3:20])[CH2:18][CH2:17][C:16](=O)[CH2:15][CH2:14]1.C([O-])(=O)C.[Na+]>ClCCl>[Cl:8][C:16]1[CH2:17][CH2:18][C:13]([O:12][CH3:11])([CH3:20])[CH2:14][C:15]=1[CH:3]=[O:4]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
Dimethylformamide (1.298 mL) in dichloromethane (2.0 mL) at −10° C. was treated dropwise with POCl3 (1.426 mL) to give a colorless solution. The mixture was stirred 5 minutes and then warmed to room temperature and stirred 30 minutes. The solution was cooled to −10° C., treated dropwise with a solution of 4-methoxy-4-methylcyclohexanone (1.74 g) in dichloromethane (2.5 mL), and stirred for 4 hours at ambient temperature. The reaction mixture was poured over a mixture of ice and 25% aqueous sodium acetate solution. After the ice melted, the reaction mixture was poured into a separatory funnel and extracted with diethyl ether (4×125 mL). The diethyl ether extracts were washed with NaHCO3 solution and brine, dried (MgSO4), filtered and concentrated. The concentrate was chromatographed on silica gel with 0 to 5% ethyl acetate in hexanes as the eluent.
Workup
- customto give a colorless solution
- stirringstirred 30 minutes
- temperatureThe solution was cooled to −10° C.
- stirringstirred for 4 hours at ambient temperature
- additionthe reaction mixture was poured into a separatory funnel
- extractionextracted with diethyl ether (4×125 mL)
- washThe diethyl ether extracts were washed with NaHCO3 solution and brine
- dry with materialdried (MgSO4)
- filtrationfiltered
- concentrationconcentrated
- customThe concentrate was chromatographed on silica gel with 0 to 5% ethyl acetate in hexanes as the eluent
Sources & evidence
- ORD record
- ord-8c8fa8869d334d68b18615ab1268c654
- Source dataset
- uspto-grants-2013_10
- Patent number
- US08546399B2
Reaction notes
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