HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,4-Dioxa-8-azaspiro(4.5)decane → HCID 19428519, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,4-Dioxa-8-azaspiro(4.5)decane | HCID 67435 | — |
| Reactant | HCID 19428547 | HCID 19428547 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 19428519 | HCID 19428519 | — |
Reaction Steps
After dissolving 2.0 g (6.89 mmoles) of 2-(4,4-ethylenedioxy-1-piperidinyl)-4,6-dichloropyrimidine in 40 ml of n-butanol and adding 2.6 ml (17.23 mmoles) of 1,4-dioxa-8-azaspiro[4,5]decane, the reaction mixture is boiled under reflux for 4 hours, then evaporated. The residue is distributed between 50 ml of chloroform and 5 ml of 10% sodium hydroxide solution. After separation the organic phase is washed 4 times with 10 ml of water each, dried and evaporated. After recrystallization from hexane the title compound is obtained in a yield of 2.51 g (91.8%)d, m.p.:130°-131° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05547949 |
| Source dataset | uspto-grants-1996_08 |
| ORD ID | ord-36da90f55f0347d5bccacab1fdffb717 |
| Source note | uspto-grants-1996_08 |