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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1980071Generated: November 2, 2026

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

https://huagongshe.com/reaction/1980071

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) was subjected to catalytic reduction with hydrogen under room temperature and atmospheric pressure until a designed amount of hydrogen was absorbed. The catalyst was removed by filtration, and the filtrate was concentrated. The residue was extracted with ether, and the ether layer was 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 numberUS04484941
Source datasetuspto-grants-1984_11
ORD IDord-a77c7c47f5654ba58048a8898e29767f
Source noteuspto-grants-1984_11