HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → Methyl 3-(benzyloxy)-5-hydroxybenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Methyl 3,5-Dihydroxybenzoate | HCID 75076 | — |
| Product | Methyl 3-(benzyloxy)-5-hydroxybenzoate | HCID 7472028 | — |
Reaction Steps
The subtitle compound was prepared from methyl 3,5-dihydroxybenzoate (5 g) and benzyl bromide (3.6 ml) by the method of example 11 step (i). Purification was by chromatography eluting with 30% ethyl acetate in isohexane. Yield 2.31 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06200981B1 |
| Source dataset | uspto-grants-2001_03 |
| ORD ID | ord-4ecb22e1e92a4d2997507054d450208c |
| Source note | uspto-grants-2001_03 |