HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 611791Generated: November 3, 2026
Dichloromethane → HCID 19597325, compound
https://huagongshe.com/reaction/611791
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Reactant | 1-Phenylpiperidin-2-one | HCID 571760 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | HCID 86754951 | HCID 86754951 | — |
| Reactant | HCID 86754952 | HCID 86754952 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19597325 | HCID 19597325 | — |
Reaction Steps
A solution of 1-phenyl-2-piperidinone from Step F in THF is added to a solution of one equivalent of LDA in THF at -78° C., and stirred for 30 min. A solution of 4-(3-hydroxy-1-propyl)-3-(1-triphenylmethyl-4--imidazolyl)propionate in methylene chloride is cooled to -78° C. under nitrogen. One equivalent of n-butyl lithium followed by one equivalent of triflic anhydride is added, the reaction stirred for 10 min, then added to the LDA/1-phenyl-2-piperidinone solution. The reaction is warmed to room temperature, and quenched with saturated ammonium chloride. The reaction is then partitioned between ethyl acetate and saturated brine. The organic phase is dried over magnesium sulfate, filtered and concentrated. The title compound is isolated by chromatography on silica gel.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06001835 |
|---|
| Source dataset | uspto-grants-1999_12 |
|---|
| ORD ID | ord-3ff37114aab5401299f0f41dcaff05d9 |
|---|
| Source note | uspto-grants-1999_12 |
|---|