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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1291118Generated: October 30, 2026

1-Benzyl-piperidin-4-yl 4-iodo-2-nitrobenzoate → 1-Benzyi-piperidin-4-yl 4-iodo-2-amino-benzoate

https://huagongshe.com/reaction/1291118

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyl-piperidin-4-yl 4-iodo-2-nitrobenzoateHCID 18919754—
CatalystIronHCID 23925—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
Product1-Benzyi-piperidin-4-yl 4-iodo-2-amino-benzoateHCID 1891976495%

Reaction Steps

0.26 g (0.000588 mol) of 1-benzyl-piperidin-4-yl 4-iodo-2-nitro-benzoate was dissolved in 3.3 ml of ethanol, diluted with 3.3 ml of acetic acid and treated with 0.123 g (0.0022 mol) of iron powder. The mixture was boiled at reflux for 4 hrs., the solvent was distilled off, the residue was taken up in ethyl acetate, washed with saturated sodium carbonate solution and sodium chloride solution and the organic phase was dried over sodium sulfate. The residue was chromatographed on silica gel with ethyl acetate/hexane (1:4) as the eluent. 0.232 g (95%) of 1-benzyi-piperidin-4-yl 4-iodo-2-amino-benzoate was obtained as a yellow oil. MS: me/e=437 (C19H22IN2O2 +).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05753679
Source datasetuspto-grants-1998_05
ORD IDord-dcf673ddcf6b415f9c683b6886eb0eee
Source noteuspto-grants-1998_05