HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuric Acid → 1-[1-(4-Aminophenyl)-2-dimethylaminoethyl]cyclohexanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | HCID 13520352 | HCID 13520352 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-[1-(4-Aminophenyl)-2-dimethylaminoethyl]cyclohexanol | HCID 13520329 | 80.5% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
5.0 g (0.018 mole) of the above amide was dissolved in 300 ml of dry tetrahydrofuran and added dropwise to a mixture of 1.1 g of lithium aluminum hydride and 8.0 ml of concentrated sulfuric acid in 200 ml of tetrahydrofuran at 0° C. The mixture was stirred at 0° C. for five hours, then the excess reagent was destroyed by the dropwise addition of 4 ml of 50:50 THF-water, then 4 ml of 15% aqueous sodium hydroxide and finally 4 ml of water. The mixture was filtered and the precipitate washed several times with THF. The combined filtrates were evaporated and the residue recrystallized from isopropanol to give 3.8 g of the title compound as the free base. Treatment with excess oxalic acid in ethyl acetate gave the dioxalate, m.p. 105° C.(d).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04535186 |
| Source dataset | uspto-grants-1985_08 |
| ORD ID | ord-845c09403a8b4b9aa950ad876b7627de |
| Source note | uspto-grants-1985_08 |