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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2110493Generated: November 4, 2026

Ethanol → 4-Chloro-3-iodoaniline

https://huagongshe.com/reaction/2110493

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-Chloro-2-iodo-4-nitrobenzeneHCID 312714—
CatalystIronHCID 23925—
SolventTetrahydrofuranHCID 8028—
Product4-Chloro-3-iodoanilineHCID 21874954—

Reaction Conditions

Temperature22 °C

Reaction Steps

1-Chloro-2-iodo-4-nitro-benzene (2.00 g, 7.09 mmol) was dissolved in THF (30 mL) at 60° C. and EtOH (35 mL) was added followed by NH4Cl (0.569 g, 10.6 mmol in 30 mL of water) and iron powder (1.58 g, 28.4 mmol). This mixture was stirred vigorously for 3 h and then cooled in 22° C. and filtered though celite rinsing with EtOAc. The solution was then concentrated to ˜30 mL in vacuo and then poured into a 1:1 solution of 1N NaOH/brine (100 mL). This mixture was then extracted with EtOAc (3×50 mL) and the organics were dried over anhydrous MgSO4. Filtration and concentration gave compound 801B as a yellow solid. No purification was necessary. HPLC: 100% at 2.310 min (retention time) (YMC S5 ODS column 4.6×50 mm eluting with 10-90% aqueous methanol over 4 mincontaining 0.2% phosphoric acid, 4 mL/min, monitoring at 220 nm), MS (ES): m/z 517.6 [M+Na]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07517904B2
Source datasetuspto-grants-2009_04
ORD IDord-7fde067f351b4bb8b440cd8d8ec6942c
Source noteuspto-grants-2009_04