HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 68294314, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Di-tert-butyl azodicarboxylate | HCID 97268 | — |
| Reactant | 1-Methyl-4-piperidinemethanol | HCID 271971 | — |
| Reactant | HCID 68295278 | HCID 68295278 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68294314 | HCID 68294314 | 84% |
Reaction Steps
Triphenylphosphine (393 mg, 1.5 mmol) and (E)-methyl 3-(1H-pyrazol-4-yl)acrylate, prepared as described above, (12 mg, 1 mmol) were added to a solution of N-methyl-4-hydroxymethyl-piperidine (165 mg, 1.25 mmol) in tetrahydrofuran (THF, 2 mL). After addition of di-tert-butyl azodicarboxylate (345 mg, 1.5 mmol), the reaction was stirred overnight at room temperature. Solvents were evaporated under reduced pressure and the residue was purified by silica gel chromatography using a gradient of Hexane in EtOAc from 1:1 to 0:100 v/v. Fractions containing product were pooled and evaporated to give 220 mg of pure material (0.84 mmol, 84%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08957066B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-eb1833eaac4b4f5d9df9114d5309d980 |
| Source note | uspto-grants-2015_02 |