HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Propanediol → 2-(3-Bromopropyl)-1,3-dioxane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Propanediol | HCID 10442 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | 4-Bromobutyraldehyde | HCID 3016005 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(3-Bromopropyl)-1,3-dioxane | HCID 14063395 | — |
Reaction Steps
To a solution of 4-bromobutanal (prepared as described in J. Org. Chem., 1979, 44, 3230-3238: 450 mg, 2.98 mmol) in tetrahydrofuran (10 mL) at room temperature was added 1,3-propane diol (1.0 mL, 13.7 mmol) and p-toluenesulfonic acid monohydrate (50 mg, 0.26 mmol). The mixture was heated at reflux for 2 hours, cooled and suspended in a mixture of water and diethyl ether (200 mL of 1:1). The two layers were separated and the organic layer was dried over magnesium sulfate, filtered, and then concentrated in vacuo to give the title compound as a clear oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06518282B1 |
| Source dataset | uspto-grants-2003_02 |
| ORD ID | ord-e76a2a4df3204d018586886af83cad7b |
| Source note | uspto-grants-2003_02 |