HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Methyl-N-Methoxy-4-(3-indolyl)butyramide → Benzyl-3-(3-indolyl)propyl ketone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Methyl-N-Methoxy-4-(3-indolyl)butyramide | HCID 11107631 | — |
| Reactant | HCID 178418336 | HCID 178418336 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Benzyl-3-(3-indolyl)propyl ketone | HCID 57064264 | 68.6% |
Reaction Steps
To a solution of 147 mg (0.60 mmol) of amide 139 in 4.0 mL of THF at -78° C. was added 1.31 mL (1.31 mmol) of benzylmagnesium chloride (1.0M in Et2O) and the reaction mixture was allowed to warm to room temperature and stir for 3 h. The reaction was quenched with 5% KHSO4 and extracted into ether. The combined ethereal layers were washed with brine and dried over MgSO4. Flash chromatography (elution with 25% ether in hexane) gave 108 mg of the ketone 140. 1H NMR consistent with structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05723459 |
| Source dataset | uspto-grants-1998_03 |
| ORD ID | ord-70019092bb2c48d18020b5be4b31c9ad |
| Source note | uspto-grants-1998_03 |