Reaction equation
[C:1]1([CH:7]([C:11]([OH:13])=[O:12])[C:8]([OH:10])=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.S(Cl)(Cl)=O.[CH:18]1(O)[CH2:23][CH2:22][CH2:21][CH2:20][CH2:19]1>CCOCC.CN(C)C=O>[C:1]1([CH:7]([C:11]([OH:13])=[O:12])[C:8]([O:10][CH:18]2[CH2:23][CH2:22][CH2:21][CH2:20][CH2:19]2)=[O:9])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1Participants
6
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
Phenylmalonic acid (13.5 g, 0.07 mol) in dry ether (40 mL) was treated with thionyl chloride (8.92 g, 5.4 mL, 0.07 mol) and one drop of N,N-dimethylformamide. The mixture was heated at 40°-50° C. for 3 hours. The clear solution was distilled under vacuum. The oily residue was redissolved in dry ether (40 mL), the solution was treated with cyclohexyl alcohol (0.075 mol), 7.9 mL) and refluxed for 2 hours. The mixture was worked up as before to give an oily product which crystallized on standing. Recrystallization was carried out from a benzene-petroleum ether (40°-60°) mixture to give a white crystalline product.
Workup
- temperatureThe mixture was heated at 40°-50° C. for 3 hours
- distillationThe clear solution was distilled under vacuum
- dissolutionThe oily residue was redissolved in dry ether (40 mL)
- temperaturerefluxed for 2 hours
- customto give an oily product which
- customcrystallized
- customRecrystallization
- customwas carried out from a benzene-petroleum ether (40°-60°) mixture
- customto give a white crystalline product
Sources & evidence
- ORD record
- ord-4f01c620be9f4001a84e5ba6c5b4be16
- Source dataset
- uspto-grants-1997_04
- Patent number
- US05618826
Linked notes
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