HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Disulfide → 1-Acetyl-4-(isothiocyanatomethyl)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | 1-(4-(Aminomethyl)piperidin-1-yl)ethan-1-one | HCID 12687022 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Acetyl-4-(isothiocyanatomethyl)piperidine | HCID 15611590 | 100% |
Reaction Steps
To a stirred and cooled (-10° C.) mixture of 41.6 parts of N,N'-methanetetraylbis[cyclohexanamine], 101 parts of carbon disulfide and 450 parts of tetrahydrofuran was added dropwise a solution of 31.2 parts of 1-acetyl-4-piperidinmethanamine in 90 parts of tetrahydrofuran. Upon completion, stirring was continued overnight at room temperature. The reaction mixture was evaporated. 2,2'-Oxybispropane was added to the residue. The precipitate was filtered off and the filtrate was evaporated, yielding 40 parts (100%) of 1-acetyl-4-(isothiocyanatomethyl)piperidine as a residue (intermediate 10).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04749702 |
| Source dataset | uspto-grants-1988_06 |
| ORD ID | ord-1337f970bdae4f528bf07a13cbb69d57 |
| Source note | uspto-grants-1988_06 |