HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Dibromo-2-propanol → 2-(2-bromo-1-(bromomethyl)ethoxy)tetrahydro-2H-pyran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Dibromo-2-propanol | HCID 7287 | — |
| Reactant | 3,4-dihydro-2H-pyran | HCID 8080 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-(2-bromo-1-(bromomethyl)ethoxy)tetrahydro-2H-pyran | HCID 11623607 | — |
Reaction Steps
To a mixture of 10 g of 1,3-dibromopropan-2-ol, 5.0 ml of 3,4-dihydro-2H-pyran and 50 ml of chloroform was added a catalytic amount of p-toluenesulfonic acid monohydrate followed by stirring at room temperature for 3 hours. The reaction solution was concentrated, diluted with diethyl ether and washed with saturated sodium bicarbonate and brine. The resulting organic layer was dried over magnesium sulfate and filtered, and the filtrate was concentrated to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07834018B2 |
| Source dataset | uspto-grants-2010_11 |
| ORD ID | ord-e4cd6d9310d74bccbd04071bffa0acb4 |
| Source note | uspto-grants-2010_11 |