HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → Methyl 5-acetyl-2,4-bis-benzyloxybenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 5-acetyl-2,4-dihydroxybenzoate | HCID 12482079 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Methyl 5-acetyl-2,4-bis-benzyloxybenzoate | HCID 11955869 | 97.3% |
Reaction Steps
To a stirred solution of benzyl bromide (16.14 L, 136 mol) and anhydrous potassium carbonate (20.25 Kg, 147.6 mol) in acetonitrile (184.5 L) was added methyl 5-acetyl-2,4-dihydroxybenzoate (14 Kg, 66.6 mol, step 2) in 6 portions over 5 h. The mixture was stirred and held at reflux for 20 hours, cooled to room temperature the mixture was poured onto water (682 L) and stirred vigorously for 2 hours. The solids were collected by centrifugation and dried under reduced pressure to constant mass in a vacuum oven at 60° C. overnight to afford methyl 5-acetyl-2,4-bis-benzyloxybenzoate (23.5 Kg, 97.3%) as a cream solid mp 114-115° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08653084B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-3e10ac7e8ca84803a5dd194714402198 |
| Source note | uspto-grants-2014_02 |