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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1744905Generated: November 1, 2026

4-Iodo-o-toluidine → 4-Chloro-2-(1H-tetrazol-5-yl)-(4-iodo-2-methyl-phenyl)-amine

https://huagongshe.com/reaction/1744905

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Iodo-o-toluidineHCID 83221—
ReactantLithium diisopropylamideHCID 2724682—
ReactantDichloromethane methanolHCID 21226129—
ReactantHCID 178505771HCID 178505771—
SolventTetrahydrofuranHCID 8028—
Product4-Chloro-2-(1H-tetrazol-5-yl)-(4-iodo-2-methyl-phenyl)-amineHCID 17842168148%

Reaction Steps

To a solution of 2-methyl-4-iodoaniline (3.52 g, 0.0151 mol) in THF (25 mL) at −78° C., LDA (2 molar solution in THF, 11.33 mL, 0.02267 mol) was added dropwise. After stirring for 0.5 hours, a solution of 1-(tetrazol-5-yl)-2-fluoro-5-chlorobenzene (1.5 g, 0.00756 mol) in THF (15 mL) was added dropwise. The reaction was stirred for 16 hours as it warmed up to room temperature. The reaction mixture was quenched with aqueous conc. NH4Cl solution and extracted with CH2Cl2. The organic layer was dried (MgSO4) and the solvent removed giving a crude product as an oil. The oil with CH2Cl2->CH2Cl2:MeOH (9.7:0.3) gave 1.5 g (48%) of the desired product: mp 205-208;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07019033B2
Source datasetuspto-grants-2006_03
ORD IDord-31eca280af42457f8d6032fb195a6226
Source noteuspto-grants-2006_03