Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1441870Generated: October 31, 2026

Ethanol → 4-Chloro-3-iodoaniline

https://huagongshe.com/reaction/1441870

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 numberUS07655689B2
Source datasetuspto-grants-2010_02
ORD IDord-2b2c515266d04e2ba4cf3f3d2f1342f2
Source noteuspto-grants-2010_02