HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → HCID 12815922, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 4-chloro-N-methylpiperidine | HCID 79342 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | HCID 12815914 | HCID 12815914 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 12815922 | HCID 12815922 | 100% |
Reaction Steps
A solution of the Grignard reagent is prepared by reaction of 2.5 g of magnesium with 13.35 g of 1-methyl-4-chloropiperidine (reference above) in 80 ml of tetrahydrofuran in the usual manner. Over 15 minutes with stirring, a solution of 18.2 g of 2-(2-fluorophenylthio)-5-methoxybenzaldehyde in 40 ml tetrahydrofuran is added dropwise and the mixture refluxed for 4 hours. After cooling, it is decomposed with 20% ammonium chloride solution and extracted with benzene. The extract is dried with potassium carbonate and evaporated. There are obtained 23.7 g (100%) crude oily α-(1-methyl-4-piperidyl)-2-(2-fluorophenylthio)-5-methoxybenzyl alcohol which is used for further work without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04431808 |
| Source dataset | uspto-grants-1984_02 |
| ORD ID | ord-ef0da2ec374247c38e723c0266c4ce1e |
| Source note | uspto-grants-1984_02 |