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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1841523Generated: November 3, 2026

Ethyl 4-amino-3-iodobenzoate → (4-Amino-3-iodophenyl)methanol

https://huagongshe.com/reaction/1841523

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-amino-3-iodobenzoateHCID 459320—
ReactantDiisobutylaluminumhydrideHCID 21225700—
SolventDichloromethaneHCID 6344—
Product(4-Amino-3-iodophenyl)methanolHCID 22724559—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of ethyl 4-amino-3-iodobenzoate (8.0 g) in CH2Cl2 (56 mL) cooled to 0° C. is added diisobutylaluminum hydride in CH2Cl2 (110 mL of a 1M solution). The reaction is stirred at 0° C. for 2 h then quenched by the addition of MeOH (50 mL). To this is added 1N HCl (100 mL). The mixture is concentrated to remove the organics. The aqueous solution is extracted with CH2Cl2 (3×). The combined organic layers are dried over Na2SO4, filtered and condensed. The resulting residue is adsorbed onto silica and chromatographed (Biotage flash 40M, gradient from CH2Cl2 to 2% MeOH/CH2Cl2). Fractions homogeneous by TLC are combined and condensed to afford (4-amino-3-iodophenyl)methanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06683181B2
Source datasetuspto-grants-2004_01
ORD IDord-c6c138aba1374098be5d75bcbcd7f040
Source noteuspto-grants-2004_01