HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → 2-(4-Bromothiophen-2-yl)-1,3-dioxolane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 4-Bromothiophene-2-carbaldehyde | HCID 87792 | — |
| Product | 2-(4-Bromothiophen-2-yl)-1,3-dioxolane | HCID 3857255 | 72% |
Reaction Steps
In a 100 mL roundbottom flask equipped with a dean stark trap and a reflux condenser, 4-bromothiophene-2-carboxaldehyde (25 g, 131 mMol) and a catalytic amount of p-toluenesulfonic acid were dissolved in benzene (50 mL). The mixture was heated to reflux overnight. The reaction was cooled, washed with sat'd sodium bicarbonate, water, dried (MgSO4) and concentrated. Purification by fractional distillation (80°-90° C., 0.5 mm Hg) afforded 24.23 g (72%) of the desired dioxolane as a clear liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05185363 |
| Source dataset | uspto-grants-1993_02 |
| ORD ID | ord-410fc2c968474776b0367118b95eccbe |
| Source note | uspto-grants-1993_02 |