HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylamine → HCID 13137236, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylamine | HCID 6341 | — |
| Reactant | HCID 13137234 | HCID 13137234 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 13137236 | HCID 13137236 | 97.1% |
Reaction Steps
Into a four-necked flask equipped with a stirrer and a thermometer, a 30% aqueous solution of monoethylamine (70 g) and tetrahydrofuran (18 g) were charged, and then 2-n-pentyl-3-hydroxy-3-methyl-4-cyclopentenone (18.2 g) was dropwise added thereto at a temperature of 10° to 20° C. for 30 minutes. At the same temperature, the reaction mixture was kept for 2 hours. After completion of the reaction, the mixture was extracted with toluene, and the organic layer was washed with water. From the organic layer, toluene was evaporated off to give 2-n-pentyl-3-methyl-4-ethylamino-2-cyclopentenone (20.3 g). Yeild, 97%. The product was purified by alumina chromatography using toluene-ethyl acetate (10:1 by volume). nD20 1.4864.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04665174 |
| Source dataset | uspto-grants-1987_05 |
| ORD ID | ord-e92a4b6c6f7e4f44b0a80d39ae35877c |
| Source note | uspto-grants-1987_05 |