Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzothiazole | HCID 7222 | — |
| 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 44239811 | HCID 44239811 | 30% |
Reaction Steps
H2O2 (30% in H2O; 0.31 mL, 3.0 mmol) was added dropwise over 1-2 min to a stirred solution of benzothiazole 1f (108 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 60 °C. 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 60 °C 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 at 60 °C for 60 min. After allowing to cool, the mixture was 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 - 7 -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 benzothiazole 1f (60 mg, 44%), and the desired product 2f (58 mg, 30%).
Provenance & Evidence
| DOI | 10.1021/jo9010624 |
|---|
| Source dataset | Minisci dataset from Roche |
|---|
| ORD ID | ord-065a25a8e27e42e0a91bfb691ac92afa |
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| Source note | Minisci dataset from Roche |
|---|