HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → HCID 14054320, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 14054310 | HCID 14054310 | — |
| Reactant | Cyclohexane ethylacetate | HCID 21867204 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Thionyl Chloride | HCID 24386 | — |
| Product | HCID 14054320 | HCID 14054320 | — |
Reaction Steps
The reaction is carried out as in Example 1, but starting with 7-phenylbenzo[b]thiophene-5-carboxylic acid (2.5 g) in toluene (25 cc) and thionyl chloride (2.2 cc) and then triethylamine (4.15 cc) and piperidine (0.97 cc) in toluene (25 cc). After two successive chromatographies of the residue on silica gel, the first with a cyclohexane:ethyl acetate (80:10:10 by volume) mixture as the eluent and the second with a cyclohexane:ethyl acetate (70:30 by volume) mixture as the eluent, a residue is isolated, which is stirred for 1 hour in 40°-60° petroleum spirit. After filtering and drying, 1-[(7-phenylbenzo[b]thien-5-yl)carbonyl]piperidine (1.55 g), m.p. 112° C., is isolated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04808599 |
| Source dataset | uspto-grants-1989_02 |
| ORD ID | ord-0de56bbb7a01437daf97e348252b755d |
| Source note | uspto-grants-1989_02 |