HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 20372282, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 20372213 | HCID 20372213 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 20372282 | HCID 20372282 | — |
Reaction Steps
By following essentially the same procedures described in Example 6, N-[α,α-dimethyl-4-(p-methyl-α,α,β,β-tetrafluorophenethyl)-benzyl]-formamide is reduced to 4-(p-methyl-α,α,β,β-tetrafluorophenethyl)-α,αN-trimethylbenzylamine. The crude oily base is converted to the hydrochloride salt by treating a solution in ethanol with a slight excess of 8N hydrogen chloride in ethanol. Dilution with absolute ether precipitates the white crystalline hydrochloride, m.p. 189°-190° C. The melting point is unchanged by recrystallization from isopropyl alcohol-ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04071570 |
| Source dataset | uspto-grants-1978_01 |
| ORD ID | ord-6af65fa3881040c7ac1539535e18e6d6 |
| Source note | uspto-grants-1978_01 |