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
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 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08530504B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-02496be81bb3406ea0711670738f8315 |
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| Source note | uspto-grants-2013_09 |
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