HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butyl 3-oxo-2-phenylpiperidine-1-carboxylate → HCID 19379354, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butyl 3-oxo-2-phenylpiperidine-1-carboxylate | HCID 11414684 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19379354 | HCID 19379354 | — |
Reaction Steps
A solution of 1-t-butoxycarbonyl-2-phenyl-piperidin-3-one (0.57 g, Example 48a)in 5 ml anhydrous tetrahydrofuran at -78° C. was treated with methyl magnesium bromide (1.6 ml of 1.5M solution in toluene-THF). The reaction was partitioned between saturated ammonium chloride-diethyl ether, the organic phase dried and evaporated in vacuo. The residue was chromatographed using 20% ethyl acetate in hexane as eluant to give 1-t-butoxycarbonyl, 3-methyl-2-phenyl piperidin-3-ol as a crystalline solid, m.p.=95°-97° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05459270 |
| Source dataset | uspto-grants-1995_10 |
| ORD ID | ord-ef5917e872314a859669994d23f119e2 |
| Source note | uspto-grants-1995_10 |