Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Azacyclonol | HCID 15723 | — |
| Reactant | 3-Methoxybenzyl chloride | HCID 69994 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 14851351 | HCID 14851351 | 102.2% |
Reaction Steps
A mixture of 8.0 g (30 mmol) of α,α-diphenyl-4-piperidinomethanol, 2.35 g (15 mmol) of 3-methoxybenzyl chloride, 0.5 g of triethylamine and 30 ml of THF is stirred under reflux for 1 hour, during which a colorless precipitate separates out. After cooling to 20° C., the precipitate is filtered off, and the filtrate is concentrated. For working up, the residue is taken up in 5 ml of methylene chloride, and ethereal HCl solution is added until no further precipitation occurs. The mixture is diluted with 30 ml of methylene chloride, the precipitate is filtered, and the filtrate is concentrated. Drying of the oily residue at 40° C. in vacuo results in 6.5 g of final product. Decomposition point about 80° C. Characteristic IR bands: 3360, 1590, 1480, 1438, 1256, 690 cm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05077301 |
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| Source dataset | uspto-grants-1991_12 |
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| ORD ID | ord-8c3b903e8ed64d9ab6549ed108c9bed6 |
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| Source note | uspto-grants-1991_12 |
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