HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium bisulfate → 5-(3-Benzyloxy-propyl)-piperidine-2,4-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium bisulfate | HCID 516920 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | Benzyl 3-Bromopropyl Ether | HCID 2776064 | — |
| Reactant | tert-Butyl 2,4-dioxopiperidine-1-carboxylate | HCID 23730999 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-(3-Benzyloxy-propyl)-piperidine-2,4-dione | HCID 69075313 | 82% |
Reaction Steps
To a solution of tert-butyl 2,4-dioxopiperidine-1-carboxylate (3.84 g, 18 mmol) in anhydrous THF (100 mL), cooled at −20° C. under nitrogen atmosphere, 1M LiHMDS in THF (54 mL) was added dropwise. After 20 min under stirring, (3-bromo-propoxymethyl)-benzene (54 mmol) was added and the solution was stirred at −20° C. for 2 hours. The reaction mixture was poured into 5% aq. KHSO4 and extracted with DCM two times. The collected organic layers were concentrated to 500 mL and 50 mL of TFA were added. The resulting solution was stirred at room temperature for 1 hour. After evaporation, the residue was purified by column chromatography (hexane/EtOAc 1:2) affording 3.85 g of the title compound (14.7 mmol, 82%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07618982B2 |
| Source dataset | uspto-grants-2009_11 |
| ORD ID | ord-7f306e4980874d0fb9b4004766e54f37 |
| Source note | uspto-grants-2009_11 |