HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → 2-(N-Benzylmethylamino)-methyl-1-(3-methoxybenzyl)cyclohexanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 3-Methoxybenzyl chloride | HCID 69994 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 2-(N-Benzylmethylamino)-methyl-cyclopentanone hydrochloride | HCID 20534820 | — |
| Product | 2-(N-Benzylmethylamino)-methyl-1-(3-methoxybenzyl)cyclohexanol | HCID 20534818 | — |
Reaction Steps
67 g (0.25 mole) of 2-(N-benzylmethylamino)methylcyclohexanone hydrochloride obtained as described in (a) are introduced in the course of 30 minutes, whilst stirring and cooling, into a Grignard solution which has been prepared from 110 g (0.7 mole) of 3-methoxybenzyl chloride, 16.8 g of magnesium and 700 ml of dry ether; stirring is continued for 16 hours at room temperature, the reaction mixture is decomposed with an excess of concentrated ammonium chloride solution, the ether layer is separated off and dried with sodium sulfate, the ether is driven off and the residue is distilled under reduced pressure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04336263 |
| Source dataset | uspto-grants-1982_06 |
| ORD ID | ord-8c5ce06aa4964f2aa00319102a5e8b47 |
| Source note | uspto-grants-1982_06 |