Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 18461181 | HCID 18461181 | — |
| Reactant | HCID 59904576 | HCID 59904576 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 59904581 | HCID 59904581 | 100% |
Reaction Steps
To a solution of 5.0 g (24 mmol) (3R,4R)-4-benzyl-3,4-dihydroxy-piperidine in 150 ml DMF were added 7.4 g (24 mmol) 1-benzyloxy-4-(2-chloro-ethoxy)-benzene and 5.0 g (36 mmol) K2CO3 and the reaction mixture was heated to 90° C. for 72 hours. After the addition of water the aqueous phase was extracted three times with ethyl acetate and the combined organic layers were washed with water, dried over MgSO4 and the solvent was removed under reduced pressure to give 10.5 g (24 mmol, 100%) (3R,4R)-4-benzyl-1-[2-(4-benzyloxy-phenoxy)-ethyl]-piperidine-3,4-diol as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06432985B1 |
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| Source dataset | uspto-grants-2002_08 |
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| ORD ID | ord-ad676a6b19e544688947195cc199039c |
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| Source note | uspto-grants-2002_08 |
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