HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 905059Generated: October 26, 2026
Imidazole → Trans-1-[6-(2,6-dichlorobenzyloxy)tetrahydropyran-2-ylmethyl]imidazole
https://huagongshe.com/reaction/905059
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | trans-6-(2,6-Dichlorobenzyloxy)-2-tosyloxymethyltetrahydropyran | HCID 54030357 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Trans-1-[6-(2,6-dichlorobenzyloxy)tetrahydropyran-2-ylmethyl]imidazole | HCID 13261936 | 94.3% |
Reaction Steps
196 mg of 55% sodium hydride were added to a solution of 306 mg of imidazole in 14 ml of dimethylformamide and the mixture was stirred at 80° C. for 30 minutes. The mixture was then cooled to room temperature, after which 1.335 g of trans-6-(2,6-dichlorobenzyloxy)-2-tosyloxymethyltetrahydropyran and 450 mg of sodium iodide were added thereto; the mixture was then stirred at 80°-85° C. for 2 hours. At the end of this time, the mixture was treated and purified essentially as described in Example 1(b), to give 965 mg of the title compound in the form of a colourless oil.
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-3e15df6b96a94f84889d4715648fdb85 |
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| Source note | uspto-grants-1983_12 |
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