Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | HCID 22620058 | HCID 22620058 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22620101 | HCID 22620101 | 36.9% |
Reaction Steps
In a Pyrex high pressure reaction tube, a solution of the preceding dioxolane (200 mg, 0.66 mmol), 140 mg (2.06 mmol) of imidazole and 90 mg (1.4 mmol) of copper powder in 1 mL of anhydrous tetrahydrofuran (THF) was stirred until homogeneous. The solvent was then evaporated under nitrogen, and the tube was sealed and heated in an oil bath at 140° C. for 16 hours. After cooling, the residue was dissolved in 20 mL of THF, filtered through a pad of diatomaceous earth and concentrated in vacuo to an oil. Chromatography on silica gel (100% ethyl acetate (EtOAc)) gave 60 mg of 2-(5-(2-imidazolyl)-2-methoxyphenyl)-1,3-dioxolane as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05854262 |
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| Source dataset | uspto-grants-1998_12 |
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| ORD ID | ord-b8831f45f7994fa6aee30fff6a91b1d4 |
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| Source note | uspto-grants-1998_12 |
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