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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1053612Generated: November 2, 2026

Methyl 2-fluoro-3-nitrobenzoate → Methyl 3-amino-2-fluorobenzoate hydrochloride

https://huagongshe.com/reaction/1053612

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 2-fluoro-3-nitrobenzoateHCID 13470961—
ReactantHydrochloride methanolHCID 21893726—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductMethyl 3-amino-2-fluorobenzoate hydrochlorideHCID 6716773185%

Reaction Steps

2-Fluoro-3-nitrobenzoic acid methyl ester (9.10 g, 0.046 mol), 10% hydrochloric acid/methanol (25 ml), methanol (60 ml), and 5% palladium/carbon (50% wet product) (2.7 g) were introduced, and the reaction mixture was hydrogenated at room temperature. After completion of the reaction, the catalyst was filtered away, and the filtrate was concentrated under reduced pressure. The concentration residue was washed with diisopropyl ether, as a result of which 8.01 g (yield: 85%) of the indicated compound was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394240B2
Source datasetuspto-grants-2016_07
ORD IDord-eb3b1a8959574d0abac47593d79546a0
Source noteuspto-grants-2016_07