HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene Glycol → HCID 15012344, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Benzene | HCID 241 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | HCID 22165514 | HCID 22165514 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 15012344 | HCID 15012344 | 90% |
Reaction Steps
A mixture of 15.6 g. (0.1 mole) of 1-acetoxy-5-hexen-2-one, 18.6 g. (0.3 mole) of ethylene glycol in 250 ml. of benzene containing 1.56 g. of p-toluene sulfonic acid monohydrate is heated to reflux using a Dean-Stark water separator. After 2 hours, the reaction mixture is shaken well with 250 ml. of cold water. The aqueous layer is washed with 3×25 ml. of ether. The combined organic layers are dried over anhydrous magnesium sulfate. Evaporation of the solvent gives 2-acetoxymethyl-2-(3-buten-1-yl)-1,3-dioxolane in 90% yield as a light brown oil. ##STR41##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04226866 |
| Source dataset | uspto-grants-1980_10 |
| ORD ID | ord-cbb50e9ebab1429a9880f09475662ab1 |
| Source note | uspto-grants-1980_10 |