HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Methyl 5-formyl-2-methanesulfonyloxybenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Methyl 5-Formylsalicylate | HCID 14363598 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 5-formyl-2-methanesulfonyloxybenzoate | HCID 23076526 | 100% |
Reaction Steps
To a mixture of methyl 5-formyl-2-hydroxybenzoate (21.76 g), triethylamine (13.46 g), ethyl acetate (300 mL) was added dropwise methanesulfonyl chloride (15.24 g) at 0° C., and the mixture was stirred at room temperature for 3 hr. The reaction mixture was washed successively with water, saturated aqueous sodium hydrogen carbonate, 1N hydrochloric acid and saturated brine, dried over anhydrous magnesium sulfate and concentrated to give methyl 5-formyl-2-methanesulfonyloxybenzoate as a colorless oil (31.20 g, yield 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07368578B2 |
| Source dataset | uspto-grants-2008_05 |
| ORD ID | ord-a52da7cf307c4afa81e4a5b0c41e419a |
| Source note | uspto-grants-2008_05 |