HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → Methyl 2-[(phenylmethyl)oxy]-5-(1-piperidinylsulfonyl)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 2-hydroxy-5-(1-piperidinylsulfonyl)benzoate | HCID 14266920 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Methyl 2-[(phenylmethyl)oxy]-5-(1-piperidinylsulfonyl)benzoate | HCID 67107209 | — |
Reaction Steps
K2CO3 (203 mg, 1.47 mmol) was added to a stirred solution of methyl 2-hydroxy-5-(1-piperidinylsulfonyl)benzoate (may be prepared as described in Description 67; 400 mg, 1.34 mmol) in acetone (20 ml), followed by the addition of (bromomethyl)benzene (251 mg, 1.47 mmol). The mixture was heated at reflux for 16 h, and then cooled to room temperature. The mixture was filtered, and the filtrate was concentrated to yield the title compound as a colourless oil. 300 mg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08778939B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-59bd5940383f46a6900231dc2e39de68 |
| Source note | uspto-grants-2014_07 |