HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 2-(2-Bromoethyl)-2,5,7,8-tetramethylchroman-6-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 2,5,7,8-Tetramethyl-6-hydroxy-2-(hydroxyethyl)chroman | HCID 11807084 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(2-Bromoethyl)-2,5,7,8-tetramethylchroman-6-ol | HCID 13375184 | 73.6% |
Reaction Steps
To 11.0 g (0.042 mol) of triphenylphosphine in 200 ml of dichloromethane is added dropwise a solution of 6.71 g (0.042 mol) of bromine in 50 ml of dichloromethane. The solution is stirred for 30 min at room temperature, then 10.0 g (0.04 mol) of 3,4-dihydro-6-hydroxy-2,5,7,8-tetramethyl-2H-1-benzopyran-2-ethanol (CAS 79907-48-5) is added. The resulting solution is refluxed for 4 hours, allowed to cool overnight, washed with a solution of 15 g of sodium carbonate in 200 ml of water, dried over anhydrous sodium sulfate, filtered and evaporated. The resulting oil is crystallized from methanol to give 9.22 g of 3,4-dihydro-2-(2-bromoethyl)-2,5,7,8-tetramethyl-2H-1-benzopyran-6-ol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05484810 |
| Source dataset | uspto-grants-1996_01 |
| ORD ID | ord-3cdcf68822c7491cba4f44d6f1696767 |
| Source note | uspto-grants-1996_01 |