HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 4-(Phenoxymethyl)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Phenol | HCID 996 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 4-(Chloromethyl)piperidine--hydrogen chloride (1/1) | HCID 12428146 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(Phenoxymethyl)piperidine | HCID 3017444 | 32.4% |
Reaction Steps
To a mixture of 28 ml of 30% sodium methanolate solution and 50 ml methanol, there are added 14.1 g (0.15 mole) of phenol. The reaction mixture is evaporated, mixed with 50 ml of N,N-dimethyl formamide and 7.8 g (0.05 mole) of 4-chloromethylpiperidine hydrochloride and heated for 18 hours at 70°-80° C. After cooling, the reaction mixture is mixed with diethyl ether, washed with water and dilute aqueous sodium hydroxide solution, dried over anhydrous sodium sulfate and evaporated in a vacuum. There are obtained 3.1 g of 4-phenoxymethylpiperidine (32% of theory); m.p. 41°-42° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04243807 |
| Source dataset | uspto-grants-1981_01 |
| ORD ID | ord-6cee14ea25ac46cbbfb76d895297a9e5 |
| Source note | uspto-grants-1981_01 |