Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Lithium iodide | HCID 66321 | — |
| Reactant | 2-(2-Bromoethoxy)tetrahydro-2H-pyran | HCID 86621 | — |
| Reactant | HCID 178418785 | HCID 178418785 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Water ethylacetate | HCID 22728543 | — |
| Product | HCID 21027721 | HCID 21027721 | — |
Reaction Steps
Imidazole-4-carboxylic acid methyl ester (756 mg, 6 mmol) was added slowly to a stirred suspension of sodium hydride (248 mg, 6.2 mmol) in tetrahydrofuran (10 mL) under nitrogen. The reaction mixture was stirred at room temperature for 30 minutes before being treated dropwise with 2-(2-bromoethoxy)-tetrahydro-2H-pyran (1.34 g, 6.4 mmol) and lithium iodide (40 mg, 0.3 mmol). The reaction mixture was allowed to stir at room temperature under nitrogen for 72 hours and then at reflux for 24 hours. The reaction mixture was cooled and diluted with a mixture of ethyl acetate:water 1:1 (300 mL). The aqueous layer was separated and extracted with ethyl acetate (2×50 mL). The organics were combined, dried over magnesium sulphate and concentrated in vacuo. The residue was purified by column chromatography on silica gel eluting with dichloromethane:methanol 100:0 to 98:2 to 96:4 to yield the title product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07056934B2 |
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| Source dataset | uspto-grants-2006_06 |
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| ORD ID | ord-45af44506fdd42588b2c455d4aceb7fb |
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| Source note | uspto-grants-2006_06 |
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