HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 21491549, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Cyclohexanone, 2-[2-(4-chlorophenyl)-2-oxoethyl]- | HCID 12270331 | — |
| Reactant | HCID 53746371 | HCID 53746371 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 21491549 | HCID 21491549 | — |
Reaction Steps
5.8 g (0.05 mole) of 2-isopropylaminopropylamine are added dropwise to a stirred solution of 12.5 g (0.05 mole) of 2-(p-chloro-phenacyl)cyclohexanone [Example 20(a)] in glacial acetic acid dropwise under nitrogen. After refluxing for 5 hours, the reaction mixture is cooled and poured into 500 ml. of water. The pH is adjusted to 1 with dilute hydrochloric acid, at which point a tan solid separates. This solid is recrystallized from methanol and then twice from an isopropanol-ether mixture to give 1-(2-isopropylaminopropyl)-2-(p-chlorophenyl)-4,5,6,7-tetrahydroindole hydrochloride as tan crystals, m.p. 192°-194° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03997557 |
| Source dataset | uspto-grants-1976_12 |
| ORD ID | ord-8ee7bf42eefd4b4f80eabd1c65b7782a |
| Source note | uspto-grants-1976_12 |