HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Toluenesulfonyl chloride → 2-Benzyloxy-5-[2-(p-toluenesulfonyloxy)ethyl]benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Benzyloxy-5-(2-hydroxyethyl)benzamide | HCID 18620067 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Benzyloxy-5-[2-(p-toluenesulfonyloxy)ethyl]benzamide | HCID 18620113 | 77% |
Reaction Steps
To a solution of 2-benzyloxy-5-(2-hydroxyethyl)benzamide (519 mg) in dichloromethane (6 ml) were added triethylamine (290 μl), N,N-dimethylaminopyridine (24 mg) and p-toluenesulfonyl chloride (400 mg) subsequently, and the mixture was stirred for 17 hours at room temperature. After concentration of the reaction mixture under reduced pressure, purification of the residue by flash column chromatography on silica gel (eluent:diethyl ether/dichloromethane=1/1) gave 2-benzyloxy-5-[2-(p-toluenesulfonyloxy)ethyl]benzamide (627 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06538152B1 |
| Source dataset | uspto-grants-2003_03 |
| ORD ID | ord-b0be7a0dacda4d0a845881967da2487c |
| Source note | uspto-grants-2003_03 |