HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(4-Phenylphenoxy)-2-hydroxypropylazide → 1-Amino-3-(biphenyl-4-yloxy)propan-2-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(4-Phenylphenoxy)-2-hydroxypropylazide | HCID 21474768 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-Amino-3-(biphenyl-4-yloxy)propan-2-ol | HCID 16642390 | 106.9% |
Reaction Steps
Hydrogen was introduced into a mixture of 2.94 g of 3-(4-phenylphenoxy)-2-hydroxypropylazide (prepared as described in Preparation 83), 0.3 g of 10% w/w palladium-on-carbon and 60 ml of ethanol for 3 hours. At the end of this time, insolubles were removed by filtration, and the filtrate was concentrated by evaporation under reduced pressure, to give 2.84 g of the title compound, melting at 137.7° to 146.8° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05688823 |
| Source dataset | uspto-grants-1997_11 |
| ORD ID | ord-518e6ce62b674bc7b42310cb778c3193 |
| Source note | uspto-grants-1997_11 |