HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene Glycol → HCID 58418115, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 5-Bromo-4-methylthiophene-2-carbaldehyde | HCID 16414192 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 58418115 | HCID 58418115 | — |
Reaction Steps
Ethylene glycol (2.18 ml) and p-toluenesulfonic acid (0.74 g) is added to a solution of 2-brom-3-methyl-5-formylthiophene (4.0 g) in toluene (98 ml) in a Dean-Stark apparatus. After 18 hours at reflux, the reaction is quenched with water. The organic phase is separated and the aqueous phase is extracted three times with ethyl acetate. The combined organic phases are dried over Na2SO4 and concentrated in vacuo. The crude product is purified on a semi-preparative HPLC to yield 2-(5-bromo-4-methyl-thiophen-2-yl)-[1,3]dioxolane (4.04 g) as a yellow oil. MS (HPLC/MS): 250 (MH+). Retention time: 4.02 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08653116B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-a2f33a69762c4e04b35517459d35e114 |
| Source note | uspto-grants-2014_02 |