Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methylquinoline | HCID 7060 | — |
| Reactant | 3-Iodooxetane | HCID 13356686 | — |
| Reagent | Hydrogen Peroxide | HCID 784 | — |
| Reagent | Sulfuric Acid | HCID 1118 | — |
| Catalyst | CID 516917 | HCID 516917 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 44239661 | HCID 44239661 | 32% |
Reaction Steps
H2O2 (30% in H2O; 0.31 mL, 3.0 mmol) was added dropwise over 1-2 min to a stirred solution of quinaldine 1b (135 μL, 1.0 mmol), concentrated H2SO4 (107 μL, 2.0 mmol), 3-iodooxetane (368 mg, 2.0 mmol) and iron(II) sulfate heptahydrate (80 mg, 0.3 mmol) in DMSO (10 mL) at room temperature. After 1-2 min a further portion of iron(II) sulfate heptahydrate (80 mg, 0.3 mmol) was added and the mixture was stirred at room temperature for 30 min. Further H2O2(0.31 mL, 3.0 mmol) and iron(II) sulfate heptahydrate (80 mg, 0.3 mmol) was added, and the mixture was stirred for 60 min, then poured into a 0.2 M solution of NaOH (30 mL) and Et2O (50 mL). The aqueous and organic layers were partitioned and the aqueous layer was extracted with Et2O (2 x 25 mL). The combined organic extracts were washed with brine (1 x 30 mL), dried (MgSO4), filtered and the solvent removed under vacuum to leave a crude oil. The oil was purified by preparative thin-layer chromatography using EtOAc / hexanes (3:7) as eluent to give recovered quinaldine 1b (55 mg, 39%), and the desired product 2b (64 mg, 32%) as a solid. An analytical portion of the product 2b was recrystallized from hexanes for data purposes.
Provenance & Evidence
| DOI | 10.1021/jo9010624 |
|---|
| Source dataset | Minisci dataset from Roche |
|---|
| ORD ID | ord-fd67d32167634289bf001446bf234950 |
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| Source note | Minisci dataset from Roche |
|---|