HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Propanediol → 2-(2-Bromophenyl)-1,3-dioxane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Propanediol | HCID 10442 | — |
| Reactant | 2-Bromobenzaldehyde | HCID 81129 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-(2-Bromophenyl)-1,3-dioxane | HCID 10847784 | — |
Reaction Steps
ortho-Bromobenzaldehyde (4a) (8 g, 43.24 mmol) was stirred with 1,3 propanediol (4.7 ml, 64.86 mmol) and p-toluenesulfonic acid monohydrate (164 mg, 0.86 mmol) in benzene (150 ml) in a flask equipped with a Dean-Stark trap and a condenser. The mixture was heated at reflux for 12 hrs, cooled, and extracted with 2 M NaOH (100 ml), and brine (100 ml×3). The solution was dried over MgSO4, and the solvent evaporated to the title compound in quantitative yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08318938B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-2392adcaa6e24e03a52a623dc451e650 |
| Source note | uspto-grants-2012_11 |