HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-(2-n-Propylpentanoyl)-1-aminoindan
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 2-Propylvaleryl chloride | HCID 76240 | — |
| Reactant | (+-)-1-Aminoindan | HCID 123445 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-(2-n-Propylpentanoyl)-1-aminoindan | HCID 11658951 | 69.3% |
Reaction Steps
A solution of valproyl chloride (1.55 g, 9.6 mmole) in toluene (25 ml) was added dropwise to a stirred and ice-cooled solution of 1-aminoindan (1.47 g, 10.0 mmole) and Et3N (1.11 g, 11 mmole). The mixture was stirred at ambient temperature for 17 hours, EtOAc (60 ml) and water (50 ml) were added and the phases were separated. The organic phase was washed successively with 0.1N HCl (40 ml), 0.1N NaHCO3 (40 ml) and saturated NaCl (40 ml), dried over magnesium sulphate and evaporated to dryness under reduced pressure. The residue was treated with hexane (15 ml, 30 min stirring, RT) and filtered. The crude product was crystallized from hexane:EtOAc (70:30 mixture), to give 1.72 g (6.65 mmole, 69%) of a white crystalline solid, mpt: 133°-4° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05639913 |
| Source dataset | uspto-grants-1997_06 |
| ORD ID | ord-2f3893689a25493d8ac0e22bf5aac241 |
| Source note | uspto-grants-1997_06 |