HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butyl 4-(3-bromophenoxy)piperidine-1-carboxylate → HCID 22492895, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butyl 4-(3-bromophenoxy)piperidine-1-carboxylate | HCID 22492957 | — |
| Reactant | Sodium methanolate methanol | HCID 23694274 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 22492895 | HCID 22492895 | — |
Reaction Steps
To a solution of tert-butyl 4-(5-bromophenyloxy)-1-piperidinecarboxylate (12.98 g) in methanol (70 ml) was added 28% sodium methoxide methanol solution (37.8 ml) and the mixture was stirred under refluxing for 4 hours. After cooling, the reaction mixture was evaporated in vacuo. The resulting residue was chromatographed on silica gel (400 ml) eluting with a mixture of n-hexane and ethyl acetate (5:1 v/v). The fractions containing the object compound were collected and evaporated under reduced pressure to give tert-butyl 4-(5-methoxypentyloxy)-1-piperidinecarboxylate (16.31 g). This compound was immediately used as the starting compound for the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06884774B2 |
| Source dataset | uspto-grants-2005_04 |
| ORD ID | ord-1353573013524c07b1d20d0d8bd2c8ae |
| Source note | uspto-grants-2005_04 |