HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → 1-(4-(1,4-Dioxaspiro[4.5]decan-8-yl)cyclohex-1-enyl)pyrrolidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | 4-(1,4-Dioxa-spiro(4.5)dec-8-yl)-cyclohexanone | HCID 810913 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(4-(1,4-Dioxaspiro[4.5]decan-8-yl)cyclohex-1-enyl)pyrrolidine | HCID 67954988 | — |
Reaction Steps
Toluene (200 ml) and pyrrolidine (90 ml) were added to 4-(1,4-dioxaspiro[4.5]decan-8-yl)cyclohexanone (100 g) in a reaction vessel equipped with a Dean-Stark apparatus under an atmosphere of nitrogen. The mixture was refluxed for 3 hours while the water formed was removed by a Dean-Stark apparatus. After the reaction mixture had been cooled to a room temperature, it was washed with brine, and dried over anhydrous magnesium sulfate. The toluene was distilled off to give 1-(4-(1,4-dioxaspiro[4.5]decan-8-yl)cyclohex-1-enyl)pyrrolidine (105.8 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08465674B2 |
| Source dataset | uspto-grants-2013_06 |
| ORD ID | ord-fb41a4f91529401aa114a48e63d90029 |
| Source note | uspto-grants-2013_06 |