HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanogen Bromide → 1-(2-Chlorophenyl)-1'-cyanospiro(indoline3,4'-piperidine)
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(2-Chlorophenyl)-1'-methylspiro[indoline-3,4'-piperidine] maleate | HCID 12801600 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 1-(2-Chlorophenyl)-1'-cyanospiro(indoline3,4'-piperidine) | HCID 12801616 | — |
Reaction Steps
To 1.0 g of 1-(2-chlorophenyl)-1'-methylspiro[indoline-3,4'-piperidine] of Example 17 in 16 ml of dry chloroform is added 2.4 g of anhydrous potassium carbonate and 0.73 g of cyanogen bromide. The reaction is stirred 7 hours at room temperature and then is filtered through paper. Approximately one ml of methanol is added and the solution is rotary evaporated to a glass. The glass is chromatographed on 80 cc of silica gel with 1:1, ether:dichloromethane to give a crystalline solid. The solid is recrystallized thrice from acetone-hexane to give a solid of 1-(2-chlorophenyl)-1'-cyanospiro(indoline-3,4'-piperidine), mp 157.5°-159.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04345081 |
| Source dataset | uspto-grants-1982_08 |
| ORD ID | ord-e6ab7b33ed5b49e89af531a59a3bf81e |
| Source note | uspto-grants-1982_08 |