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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41240Generated: October 28, 2026

Acetonitrile → Ethyl 3-chloro-4-iodo-5-methoxybenzoate

https://huagongshe.com/reaction/41240

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantDiiodomethaneHCID 6346—
ReactantIsoamyl NitriteHCID 8053—
ReactantEthyl 4-amino-3-chloro-5-methoxybenzoateHCID 57912463—
SolventEthylacetate heptaneHCID 21899848—
ProductEthyl 3-chloro-4-iodo-5-methoxybenzoateHCID 5791245166.6%

Reaction Conditions

Temperature70 °C

Reaction Steps

To ethyl 4-amino-3-chloro-5-methoxybenzoate (15.8 g, 68.8 mmol), were added acetonitrile (40 mL) and diiodomethane (22.2 mL, 275 mmol) in this order, and the mixture was stirred at 70° C., and then isoamyl nitrite (13.9 mL, 103 mmol) was added dropwise thereto over 10 minutes. The mixture was stirred at 70° C. for 40 minutes. The mixture was returned to room temperature, the solvent was then distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (a mixed solvent of n-heptane and ethyl acetate: n-heptane/ethyl acetate=8/1 then 5/1) to obtain the title compound (15.6 g, 45.8 mmol)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530504B2
Source datasetuspto-grants-2013_09
ORD IDord-02496be81bb3406ea0711670738f8315
Source noteuspto-grants-2013_09