HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 4-Piperidinol, 1-benzyl-4-phenyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 1-Chloroethyl chloroformate | HCID 521305 | — |
| Reactant | HCID 67059915 | HCID 67059915 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Piperidinol, 1-benzyl-4-phenyl- | HCID 97333 | 55% |
Reaction Steps
To 1-benzyl-4-fluoro-4-phenyl-piperidine (0.22 g) in dry DCM (5 mL) was added 1-chloroethylchloroformate (1 mmol). The mixture was stirred for 1 hour and then methanol (5 mL) was added and the mixture stirred overnight. The solvent was removed under vacuum, and the resulting solid triturated from diethyl ether to give the title compound as a white solid (0.12 g). LCMS m/z 180.1 [M+H]+. R.T.=2.27 min (Analytical Method 4).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08642621B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-58411a10c2db403f87882eee465cf485 |
| Source note | uspto-grants-2014_02 |