HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4-Piperidinemethanol, 1-benzoyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | Ethyl 1-benzoylpiperidine-4-carboxylate | HCID 735824 | — |
| Reactant | Trilithium borate | HCID 13743157 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Piperidinemethanol, 1-benzoyl- | HCID 10262870 | 90% |
Reaction Steps
10.4 g (0.04 mol) of ethyl 1-benzoyl-4-piperidine-carboxylate were dissolved in 90 ml of THF and treated with a solution of 0.871 g (0.04 mol) of lithium borate in 20 ml of THF. 0.45 ml (0.004 mol) of trimethyl borate was added and the mixture was stirred at room temperature for 60 hrs. The reaction mixture was treated with water and stirred for 1.5 hrs. The mixture was extracted with ethyl acetate and the organic phase was washed with water and saturated sodium chloride solution and dried over sodium sulfate. The residue was chromatographed on silica gel with ethyl acetate/hexane (1:1). 7.8 g (90%) of 1-benzoyl-4-hydroxymethyl-piperidine were obtained as white crystals; m.p. 84°-87°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05753679 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-7f6c9900f2484e1da42ec8aeb541153a |
| Source note | uspto-grants-1998_05 |