HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → 2-(Benzyloxy)-5-bromo-1,3-dimethylbenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Bromo-2,6-dimethylphenol | HCID 16919 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-(Benzyloxy)-5-bromo-1,3-dimethylbenzene | HCID 22963133 | — |
Reaction Steps
11.7 mL (96.5 mmol) benzylbromide were added dropwise to 20 g (96.5 mmol) 2,6-dimethyl-4-bromophenol and 16.5 g (118 mmol) potassium carbonate in 300 mL acetone and stirred overnight at RT. The precipitate formed was suction filtered, washed with acetone and the filtrate was evaporated down. The residue was dissolved in DCM, filtered through Alox and washed with DCM. The filtrate was evaporated down.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08629137B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-cfa2eed5035345cca13736a15a3ded78 |
| Source note | uspto-grants-2014_01 |