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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095114Generated: November 2, 2026

1,2-Dichloroethane → 5-Chloro-2-iodobenzaldehyde

https://huagongshe.com/reaction/1095114

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant5-Chloro-2-iodobenzoic acidHCID 139451—
ReactantBorane;tetrahydrofuranHCID 2723981—
CatalystManganese dioxideHCID 14801—
SolventTetrahydrofuranHCID 8028—
Product5-Chloro-2-iodobenzaldehydeHCID 57565882121.4%

Reaction Steps

To a solution of 5-chloro-2-iodo benzoic acid (4.92 g, 17 mmol) (TRANS) in anhydrous tetrahydrofuran (100 mL) at 0° C. was added borane tetrahydrofuran (1 M, 34 mL, 34 mmol) dropwise. The reaction mixture was then stirred at room temperature for 18 h. The mixture was concentrated and residue was partitioned between ethyl acetate and water. Organic layer was separated, washed with brine, dried over MgSO4, and concentrated to give a colorless oil. The oil was dissolved into 1,2-dichloroethane (50 mL), and activated MnO2 (15 g) was added. The mixture was then heated at reflux for 2 h, cooled to room temperature, and filtered through a short pad of celite. The filtrated was concentrated and purified by chromatography (EtOAc:hexanes=1;8) to give 5-chloro-2-Iodo-benzaldehyde as a white solid (Yield 5.5 g, 25%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08134001B2
Source datasetuspto-grants-2012_03
ORD IDord-50922ef1eefb4a759a072b93aa5de00c
Source noteuspto-grants-2012_03