HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → 5,5-Bis(bromomethyl)-2-phenyl-1,3-dioxane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 2,2-Bis(bromomethyl)-1,3-propanediol | HCID 18692 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 5,5-Bis(bromomethyl)-2-phenyl-1,3-dioxane | HCID 21823070 | 88.6% |
Reaction Steps
2,2-Bis(bromomethyl)propane-1,3-diol (250 g) and benzaldehyde (110 g) were added to benzene (500 cm3) containing concentrated sulphuric acid (2 cm3) and the mixture boiled. Water was removed using a Dean Stark apparatus. After about 6 hours the reaction was complete. The mixture was cooled and the sulphuric acid neutralised by the addition of excess sodium bicarbonate. The resulting solution was filtered and the benzene removed under reduced pressure to give an oil which solidified on standing. Recrystallisation from petroleum ether gave the 1,3-dioxane (296 g) as a white solid (m.p. 66° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04916214 |
| Source dataset | uspto-grants-1990_04 |
| ORD ID | ord-4550d0a6d92b4106909d601e2b4b7037 |
| Source note | uspto-grants-1990_04 |