HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → Methyl 6-bromo-3-hydroxy-2-methylbenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | Methyl 3-hydroxy-2-methylbenzoate | HCID 12488879 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 6-bromo-3-hydroxy-2-methylbenzoate | HCID 77058981 | 92% |
Reaction Steps
To a solution of methyl 3-hydroxy-2-methylbenzoate (114a, 3.557 g, 21.40 mmol) in dichloromethane (100 mL) in a dry ice/acetonitrile bath (˜−45° C.) was added bromine (1.15 mL, 22.5 mmol) dropwise. The reaction was stirred at −45° C. for 2 hours before Na2S2O3 (sat. aq., 2 mL) was added. The reaction mixture was allowed to warm to room temperature. The reaction mixture was diluted with dichloromethane and washed with water. The dichloromethane layer was concentrated under vacuum, and the resulting crude product was purified by column chromatography (0-40% ethyl acetate/heptane) to give methyl 6-bromo-3-hydroxy-2-methylbenzoate (114b, 4.8 g, 92% yield) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09040515B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-df2ba9b3fe8045e9b14c73f71d8c0c4d |
| Source note | uspto-grants-2015_05 |