HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 22007168, compound → 3-(2-Amino-1-hydroxyethyl)-4-methoxybenzene-1-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 22007168 | HCID 22007168 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-(2-Amino-1-hydroxyethyl)-4-methoxybenzene-1-sulfonamide | HCID 9906041 | 95.4% |
Reaction Steps
11 g (0.040 mol) of (−)-α-azidomethyl-2-methoxy-5-sulphamoylbenzenemethanol, 500 ml of ethanol and 2.2 g of 10% palladium on charcoal are introduced into a 1-liter reactor. The reactor is closed and purged with nitrogen, and the mixture is stirred under 400 kPa of hydrogen at room temperature for 3 hours. The reaction mixture is then filtered through Whatman paper, the recovered catalyst is suspended in 200 ml of methanol and the mixture is heated to boiling for 30 minutes. It is then filtered through Whatman paper, the filtrates are combined and concentrated and the residue is dried in a desiccator under vacuum over phosphorus pentoxide. 9.4 g of (−)-α-aminomethyl-2-methoxy-5-sulphamoylbenzenemethanol are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06214882B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-206430ca2e52421a9497c3df1bcb391f |
| Source note | uspto-grants-2001_04 |