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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 900511Generated: October 28, 2026

2,3-Difluoro-4-(2-phenyldiazenyl)phenol → 4-Amino-2,3-difluorophenol

https://huagongshe.com/reaction/900511

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-Difluoro-4-(2-phenyldiazenyl)phenolHCID 135574104—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product4-Amino-2,3-difluorophenolHCID 277876674.2%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07358397B2
Source datasetuspto-grants-2008_04
ORD IDord-e098fa1cc7d249be8f61aaffb36a4688
Source noteuspto-grants-2008_04