HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 6-Chloro-1-(2-fluorophenyl)spiro[indoline-3,4'-piperidine] maleate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Maleic Acid | HCID 444266 | — |
| Reactant | 6-Chloro-1'-cyano-1-(2-fluorophenyl)spiro[indoline-3,4'-piperidine] | HCID 13154050 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-Chloro-1-(2-fluorophenyl)spiro[indoline-3,4'-piperidine] maleate | HCID 12801624 | — |
Reaction Steps
A solution of 3.4 g of 6-chloro-1'-cyano-1-(2-fluorophenyl)spiro[indoline-3,4'-piperidine], Example 26, in 50 ml of tetrahydrofuran is added dropwise to a refluxing slurry of 1.0 g of lithium aluminum hydride in 50 ml of tetrahydrofuran. After total addition the mixture is stirred at reflux for 2.5 hours before being treated with water and alkali. The resulting oily product, in ether, is converted to its maleic acid salt which is recrystallized from an ethyl alcohol-ether mixture to provide off-white granules, mp 174.5°-175.5° C. of 6-chloro-1-(2-fluorophenyl)spiro[indoline-3,4'-piperidine] maleate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04307235 |
| Source dataset | uspto-grants-1981_12 |
| ORD ID | ord-e84267c525ec4855823a08ca73216539 |
| Source note | uspto-grants-1981_12 |