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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 534665Generated: October 29, 2026

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

https://huagongshe.com/reaction/534665

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 numberUS08853440B2
Source datasetuspto-grants-2014_10
ORD IDord-4ca83f54d0934a93b6ccb7a2892b52c0
Source noteuspto-grants-2014_10