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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2303911Generated: November 2, 2026

HCID 18461402, compound → HCID 18461398, compound

https://huagongshe.com/reaction/2303911

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 18461402HCID 18461402—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 18461398HCID 1846139877.4%

Reaction Steps

A mixture of N-methyl-N-[2-nitro-5-(pentafluorophenoxy)phenyl]amine (2.10 g), palladium on carbon (10%, 0.23 g) and methanol (300 ml) was stirred under a hydrogen atmosphere at ambient temperature for 4 hours. The catalyst was removed by filtration and the filtrate was concentrated. The residue was purified by chromatography on a silica gel column using n-hexane/ethyl acetate=3/1 as the eluant to give N-[2-amino-5-(pentafluorophenoxy)phenyl]-N-methylamine (1.48 g), of which Rf was 0.26 in thin layer chromatography on a silica gel plate using n-hexane/ethyl acetate=4/1. A mixture of this product, glycolic acid (0.76 g), 4N hydrochloric acid (25 ml) and dioxane (25 ml) was heated at reflux for 16 hours. The reaction mixture was concentrated and water was added to the residue. The mixture was neutralized with sodium bicarbonate and extracted with ethyl acetate. The ethyl acetate layer was dried over anhydrous sodium sulfate and concentrated. The residue was purified by chromatography on a silica gel column using ethyl acetate/methanol=20/1 as the eluant. The product was crystallized from n-hexane under irradiation of ultrasonic wave. The crystals were collected by filtration and washed with n-hexane to give the title compound (1.17 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06432993B1
Source datasetuspto-grants-2002_08
ORD IDord-a8e01dacc19348cfba75d43d80e3f437
Source noteuspto-grants-2002_08