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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1971777Generated: November 2, 2026

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

https://huagongshe.com/reaction/1971777

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 that order, and then the mixture was stirred at 70° C. and isoamyl nitrite (13.9 mL, 103 mmol) was added dropwise over a period of 10 minutes. The mixture was then stirred at 70° C. for 40 minutes. After returning the mixture to room temperature, the solvent in the mixture was distilled off under reduced pressure and the residue was purified by silica gel column chromatography (mixture 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 numberUS08431603B2
Source datasetuspto-grants-2013_04
ORD IDord-cfae15e6fc0f46c9a0f38139eac18d33
Source noteuspto-grants-2013_04