HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromobenzyl bromide → 1-Bromo-2-(methoxymethyl)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromobenzyl bromide | HCID 76965 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-Bromo-2-(methoxymethyl)benzene | HCID 12927162 | 87% |
Reaction Steps
685 g (2.74 mol) of o-bromobenzyl bromide are refluxed together with 2.74 mol of a 30% strength sodium methylate solution in methanol for 15 hours. The mixture is cooled and then concentrated, the residue is taken up in ethyl acetate, and the solution is washed with water. The organic phase is dried over sodium sulfate and then concentrated. 478.2 g (87%) of product are obtained as a colorless liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05254717 |
| Source dataset | uspto-grants-1993_10 |
| ORD ID | ord-ac990156198e4b42a08f29931fbd0efa |
| Source note | uspto-grants-1993_10 |