HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,1-Dimethoxyethyl(dimethyl)amine → HCID 20459997, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,1-Dimethoxyethyl(dimethyl)amine | HCID 87835 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3-(3-Methoxyphenyl)cyclohex-2-enone | HCID 11458340 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 20459997 | HCID 20459997 | — |
Reaction Steps
10 g of 3-(m-methoxyphenyl)-2-cyclohexen-1-ol obtained by reducing 3-(m-methoxyphenyl)-2-cyclohexene-1-one with sodium borohydride, are dissolved in 100 ml of xylene, whereupon 12 g of N,N-dimethylacetamide dimethyl acetal are added, and the mixture is boiled at reflux for 8 hours. After distillation of the solvent, the oil remaining behind is chromatographed on a 30-fold amount of silica gel. The fractions which are uniform in accordance with thin-layer chromatography and which are produced by elution with methylene chloride, are combined and evaporated, and there is obtained pure 1-(m-methoxyphenyl)-N,N-dimethyl-3-cyclohexene-1-acetamide in the form of a pale yellowish oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04336268 |
| Source dataset | uspto-grants-1982_06 |
| ORD ID | ord-4aee8ff11625442997e576c5bd4d8718 |
| Source note | uspto-grants-1982_06 |