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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1761329Generated: October 31, 2026

Phenol, 2-chloro-4-fluoro-5-nitro- → 5-Amino-2-chloro-4-fluorophenol

https://huagongshe.com/reaction/1761329

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenol, 2-chloro-4-fluoro-5-nitro-HCID 158655—
ReactantHCID 178418361HCID 178418361—
CatalystAdams' catalystHCID 345198—
SolventEthanolHCID 702—
Product5-Amino-2-chloro-4-fluorophenolHCID 15865485.3%

Reaction Steps

A suspension of 2-chloro-4-fluoro-5-nitrophenol (9.17 g) and platinum dioxide (500 mg) in ethanol (120 ml) is subjected to catalytic reduction with hydrogen at room temperature and atmospheric pressure until a designed amount of hydrogen is absorbed. The catalyst is removed by filtration, and the filtrate is concentrated. The residue is extracted with ether, and the ether layer is concentrated to obtain 6.6 g of 3-amino-6-chloro-4-fluorophenol. M.P., 145°-146° C. (decomp.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04826533
Source datasetuspto-grants-1989_05
ORD IDord-7b00c9a079854bf780b47c7053d4f9e5
Source noteuspto-grants-1989_05