HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1,2-Cyclohexanediol, 4-ethenyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 7-Oxabicyclo(4.1.0)heptane, 3-ethenyl- | HCID 7832 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1,2-Cyclohexanediol, 4-ethenyl- | HCID 147393 | — |
Reaction Steps
Into a two-neck flask (100 ml) were fed 15.9 g (128 mmol) of 4-vinylcyclohexene-1,2-epoxide, 40 ml of water, 20 ml of acetone, and 40 μl of sulfuric acid, and the reaction mixture was refluxed at 75° C. for 4 hours. After complete reaction, an object compound was extracted with each 60 ml of diethylether four times, and was washed with saturated salt solution, and then was dried with sodium sulfate. The solvent was evaporated to obtain 1,2-dihydroxy-4-vinylcyclohexane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06794528B2 |
| Source dataset | uspto-grants-2004_09 |
| ORD ID | ord-d9c81395887b4a68a55f9994d3fb913c |
| Source note | uspto-grants-2004_09 |