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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1763098Generated: October 31, 2026

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

https://huagongshe.com/reaction/1763098

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 numberUS04835324
Source datasetuspto-grants-1989_05
ORD IDord-046b973adf354ad884147b362331da6c
Source noteuspto-grants-1989_05