HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,1'-Thiocarbonyldiimidazole → 1-(4-Isothiocyanatophenyl)-4-(1-methylethyl)piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,1'-Thiocarbonyldiimidazole | HCID 80264 | — |
| Reactant | 4-[4-(Propan-2-yl)piperazin-1-yl]aniline | HCID 9161545 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(4-Isothiocyanatophenyl)-4-(1-methylethyl)piperazine | HCID 9878386 | 101.3% |
Reaction Conditions
| Temperature | -15 °C |
|---|
Reaction Steps
A solution of 4-[4-(1-methylethyl)-1-piperazinyl]benzenamine (1.6 g,˜6.8 mmol) (from Step B above) in N,N-dimethylformamide (25 mL) was added dropwise over 20 min to a cooled (−15° C.) solution of thiocarbonyldiimidazole (1.4 g, 7.7 mmol) (Aldrich) in N,N-dimethylformamide (30 mL). After the addition was complete, the mixture was stirred at −15° C. for 20 min, then the cooling bath was removed and the solution was stirred for 1 h. Ice-water was added and the mixture was extracted with ether. The ether layer was dried (MgSO4), filtered, and evaporated to give 1-(4-isothiocyanatophenyl)-4-(1-methylethyl)piperazine (1.8 g, quantitative yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07094896B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-9f2a80a91dcc4887a781077f3e4406f3 |
| Source note | uspto-grants-2006_08 |