HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene Glycol → 2-(3-Bromothiophen-2-yl)-1,3-dioxolane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 3-Bromothiophene-2-carboxaldehyde | HCID 2797079 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(3-Bromothiophen-2-yl)-1,3-dioxolane | HCID 12220211 | — |
Reaction Steps
3-bromo-2-formylthiophene (3.89 parts, 0.02M) was heated at reflux with dry ethyleneglycol (1.6 parts) toluene (25 parts) and p-toluene sulphonic acid (0.1 parts) in a vessel equipped with a Dean and Stark separator for 16 hours. The reactants were then cooled and evaporated into silica. The silica was formed into a column which was then developed by elution with hexane containing increasing amounts of dichloromethane. The product was obtained from fractions containing 10-60% dichloromethane as a pale straw-coloured oil (4.42 parts).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05880188 |
| Source dataset | uspto-grants-1999_03 |
| ORD ID | ord-9a42a9db6fe040e7a8af27860342855a |
| Source note | uspto-grants-1999_03 |