HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 69838142, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | N-Methylbenzylamine | HCID 7669 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 12424833 | HCID 12424833 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 69838142 | HCID 69838142 | — |
Reaction Steps
The 5-oxo-5-phenylpentanoic acid benzyl-methyl amide was prepared by refluxing N-methylbenzylamine (10.5 mmol) and 6-phenyl-3,4-dihydro-pyran-2-one (10.5 mmol) in toluene for one hour. The reaction was allowed to stir overnight at room temperature. It was poured into 100 mL of ethyl acetate and 100 mL of 1N HCl. The organic extracts were washed with 100 mL of 1N NaOH, 100 mL of water and dried over MgSO4. The crude product was flash chromatographed (CH2Cl2 /MeOH 98/2) to afford a liquid. 1H NMR (CDCl3) δ2.0-2.2 (m, 2H), 2.5 (t, 2H), 2.93/2.96 (s/s, 3H), 3.0-3.2 (m, 2H), 4.5/4.6 (s/s, 2H),7.1-7.6 (m, 8H), 7.8-8.0 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05789440 |
| Source dataset | uspto-grants-1998_08 |
| ORD ID | ord-32585b4a1b8845f19cc319cf0e50fdcf |
| Source note | uspto-grants-1998_08 |