HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → HCID 20357471, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Cyclobutanecarbonyl chloride | HCID 78705 | — |
| Reactant | 4-(2-Chloro-9H-thioxanthen-9-ylidene)piperidine | HCID 13319426 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 20357471 | HCID 20357471 | — |
Reaction Steps
Similarly, 6.3 g. (0.02 mol) of 4-(2-chloro-9-thioxanthenylidene)piperidine in 30 ml. of benzene is treated with a solution of 1.2 g. (0.01 mol) of cyclobutylcarboxylic acid chloride in 10 ml. of benzene. Following the above workup procedure, the intermediate amide is reduced with 1.5 g. (0.04 mol) of lithium aluminum hydride in 50 ml. of ether. After isolation of the amine product, the ether is evaporated in vacuo and a hexamate salt formed of 4-(2-chloro-9-thioxanthenylidene)-1-cyclobutylmethylpiperidine, m.p. 180°-182° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04086350 |
| Source dataset | uspto-grants-1978_04 |
| ORD ID | ord-e01276bb37d24998ae18da908969d794 |
| Source note | uspto-grants-1978_04 |