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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Diiodomethane | HCID 6346 | — |
| Reactant | Isoamyl Nitrite | HCID 8053 | — |
| Reactant | Ethyl 4-amino-3-chloro-5-methoxybenzoate | HCID 57912463 | — |
| Solvent | Ethylacetate heptane | HCID 21899848 | — |
| Product | Ethyl 3-chloro-4-iodo-5-methoxybenzoate | HCID 57912451 | 66.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08431603B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-cfae15e6fc0f46c9a0f38139eac18d33 |
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| Source note | uspto-grants-2013_04 |
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