HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Fluorophenyl 4-piperidyl ketone hydrochloride → HCID 178453902, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Fluorophenyl 4-piperidyl ketone hydrochloride | HCID 3084438 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 178453924 | HCID 178453924 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178453902 | HCID 178453902 | 95.6% |
Reaction Steps
A mixture of 4-(4-fluorobenzoyl)piperidine hydrochloride (0.850 g, 3.4 mmol), trans-[4-(2-Oxo-ethyl)-cyclohexyl]-carbamic acid tert-butyl ester (0.926 g, 4 mmol), in dichloromethane (10 mL) was stirred for 2 hours at room temperature and sodium triacetoxyborohydride (1.33 g, 6 mmol) was added and the resulting solution was stirred for 12 hours until the TLC indicated completion of the reaction. The mixture was filtrated and concentrated to dryness and purified with column chromatography on silica gel using CH2Cl2—CH2Cl2/MeOH (1-9:1). The product fractions were concentrated to give 1.4 g (3.25 mmol, 93.2% yield) of a light yellow solid. MS (m/e): 433.4 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08097637B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-b53cef4b3c12404ba0bfe816a1c769d5 |
| Source note | uspto-grants-2012_01 |