Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-(1H-imidazol-1-yl)-1-phenylethanol | HCID 32239 | — |
| Reactant | HCID 53994231 | HCID 53994231 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 54232927 | HCID 54232927 | 35.5% |
Reaction Steps
1 ml of a dimethylformamide solution containing 23 mg of 1-phenyl-2-(1-imidazolyl)ethanol was heated at 50° C. for 30 minutes with 5 mg of 55% sodium hydride, and then 1 ml of a dimethylformamide solution containing 65 mg of cis-6-(2,4-dichlorobenzyloxy)-2-tosyloxymethyltetrahydropyran, prepared as described in Example 2(a), were added thereto. The mixture was heated at 85° C. for 3 hours and then the mixture was treated and the product purified essentially as described in (a) above, to give 20 mg of the title compound as a liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04421758 |
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| Source dataset | uspto-grants-1983_12 |
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| ORD ID | ord-51a9421410af45d789c30a55203db04b |
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| Source note | uspto-grants-1983_12 |
|---|