Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | (2-(Chloromethyl)oxazol-4-yl)methanol | HCID 67958068 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67957879 | HCID 67957879 | — |
Reaction Steps
In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of (2-(chloromethyl)oxazol-4-yl)methanol (500 mg, 3.39 mmol) in CH2Cl2 (2.0 mL) was treated with EtI (0.28 mL, 3.39 mmol) followed by Ag2O (1.18 g, 5.08 mmol) and the resulting mixture (protected from light) was stirred overnight at 40° C. The reaction mixture was filtered and the solvent was removed under reduced pressure. Purification of the residue by FC (7:3 hept-EA) gave the title compound as a yellow oil: TLC: rf (7:3 hept-EA)=0.29. LC-MS-conditions 07: tR=0.62 min, [M+H]+=176.26.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846733B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-5ddf421da2d54c7cb5d9b0321fe2070e |
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| Source note | uspto-grants-2014_09 |
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