Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | HCID 13606747 | HCID 13606747 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 13606748 | HCID 13606748 | — |
Reaction Steps
A solution of 2.25 g (5.5 mm) of diethyl 1,4-dihydro-4-(2-methoxy-1-naphthalenyl)-2,6-dimethyl-3,5-pyridinedicarboxylate 20 in 12.0 mL of dry 1,2-dichloroethane was stirred under Ar at 25° C. and treated with 2.40 g (7.68 mm) of BBr3.CH3SCH3 complex. After stirring at 25° C. for 20 hours, 10.0 g of anhydrous powdered K2CO3 and 100 mL of absolute ethanol were added. Stirring was continued for 60 hours at 25°. The reaction was quenched with saturated aqueous NH4Cl and extracted with 500 ml of CH2Cl2. The organic layer was washed with pH 7 phosphate buffer and brine, dried (anhydrous Na2SO4), filtered, evaporated and flash chromatographed (silica gel, 2% acetone in CH2Cl2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04579851 |
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| Source dataset | uspto-grants-1986_04 |
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| ORD ID | ord-bd694a4f6ffc4d48af07a54c55e1e0f4 |
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| Source note | uspto-grants-1986_04 |
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