HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3-Difluoro-4-(2-phenyldiazenyl)phenol → 4-Amino-2,3-difluorophenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3-Difluoro-4-(2-phenyldiazenyl)phenol | HCID 135574104 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Amino-2,3-difluorophenol | HCID 2778766 | 74.2% |
Reaction Steps
61 g (0.26 mol) of 2,3-difluoro-4-(phenyldiazenyl)phenol from Example 3 and 1 g of Pd/C (10%) are initially charged in 800 ml of ethanol. The solution was degassed and aerated with hydrogen. The mixture was stirred at room temperature under a 1 bar hydrogen atmosphere for 18 hours. On completion of hydrogen uptake, the catalyst was filtered off and the filtrate was concentrated on a rotary evaporator, in the course of which the product already crystallized out. The resulting solid was filtered off, washed with a little cold ethanol and dried under high vacuum for 4 hours. 28 g (74%) of the desired compound were obtained as a light brown powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07358397B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-e098fa1cc7d249be8f61aaffb36a4688 |
| Source note | uspto-grants-2008_04 |