Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | HCID 53952191 | HCID 53952191 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 54448051 | HCID 54448051 | 85% |
Reaction Steps
To a solution of 23.5 g of 3-hydroxy-5-methoxy -2-methylbenzoic acid methyl ester in 1.3 l of chloroform was added over 1 h at -50° to -60° C. a solution of 19.2 g of bromine in 0.2 l of chloroform. Stirring was continued for 2.5 h at -40° C. and for 2 h at 0° C. The reaction mixture was evaporated in vacuo at 0° C.; the residue was dissolved in a mixture of toluene/ethanol (1:1, v/v) and the solvent was again evaporated in vacuo. This procedure Was repeated twice with toluene/ethanol (1:1, v/v), and finally once with toluene. The residue was chromatographed on silica gel using ethyl acetate as eluent and the pure product was crystallized from ethyl acetate to yield 28 g of 2-bromo-3-methoxy-5-hydroxy-6-methylbenzoic acid methyl ester as white crystals, m.p. 105°-110° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05589473 |
|---|
| Source dataset | uspto-grants-1996_12 |
|---|
| ORD ID | ord-30a3931f24c54bfc9777168835b9ffd8 |
|---|
| Source note | uspto-grants-1996_12 |
|---|