HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene Glycol → 3-[2-Benzyloxy-4-(1,1-dimethylheptyl)phenyl]cyclohex-3-en-1-one ethylene ketal
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Hydroquinone | HCID 785 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | 3-[2-Benzyloxy-4-(1,1-Dimethylheptyl)phenyl]cyclohex-2-enone | HCID 19855380 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 3-[2-Benzyloxy-4-(1,1-dimethylheptyl)phenyl]cyclohex-3-en-1-one ethylene ketal | HCID 57207235 | — |
Reaction Steps
A solution of 500 mg. of 3-[2-benzyloxy-4-(1,1dimethylheptyl)phenyl]cyclohex-2-en-1-one, 7.8 g. of ethylene glycol, 375 mg. of hydroquinone and 50 mg. of p-toluenesulfonic acid monohydrate in 50 ml. of benzene is heated at reflux for 12 hours using a Dean-Stark condensor filled with 3A molecular sieves. The reaction is cooled, added to 500 ml. saturated sodium bicarbonate and the quenched mixture extracted with three 150 ml. portions of ether, dried over magnesium sulfate and evaporated to a solid. This solid is purified via column chromatography on 50 g. of silica gel eluted with 50% ether-petroleum ether to yield the title product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04921994 |
| Source dataset | uspto-grants-1990_05 |
| ORD ID | ord-53d739275cab4593a28100bda7d29604 |
| Source note | uspto-grants-1990_05 |