HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(4-Nitrophenyl)thiomorpholine → 4-Thiomorpholinoaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(4-Nitrophenyl)thiomorpholine | HCID 3124725 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4-Thiomorpholinoaniline | HCID 10774206 | — |
Reaction Steps
A solution of 23.47 g of 4-(p-nitrophenyl)-tetrahydro-4H-1,4-thiazine in 1.5 l of dioxane is hydrogenated over Raney-nickel until the hydrogen uptake has finished. Thereafter, the catalyst is removed by filtration, washed well with dioxane and the filtrate is evaporated in vacuo. By recrystallization of the crude product from dichloromethane/ether, there is obtained 4-(p-aminophenyl)-tetrahydro-4H-1,4-thiazine of melting point 109°-111°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04640918 |
| Source dataset | uspto-grants-1987_02 |
| ORD ID | ord-da050e0f4637429f847234a784ccecf3 |
| Source note | uspto-grants-1987_02 |