HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(Phenylmethoxy)benzenemethanol → 3-Benzyloxybenzyl bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(Phenylmethoxy)benzenemethanol | HCID 74341 | — |
| Reactant | Bromotrimethylsilane | HCID 76113 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Benzyloxybenzyl bromide | HCID 1502047 | — |
Reaction Steps
A solution of 3-benzyloxybenzyl alcohol (2.04 g) in methylene chloride (20 mL) with TMS Bromide (2.5 eq. 3.14 mL) was heated at reflux for 6 hr. After cooling, the reaction was concentrated and then reconcentrated 2× from methylene chloride. The residue was chromatographed on silica gel with 5% methylene chloride in hexane to afford 3-benzyloxybenzyl bromide (1.26 g) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05705524 |
| Source dataset | uspto-grants-1998_01 |
| ORD ID | ord-148bdd1a9f154f59962ee4b9f4440268 |
| Source note | uspto-grants-1998_01 |