HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588856Generated: November 3, 2026
Potassium Carbonate → Methyl 2-(4-chloro-5-iodo-2-methoxyphenylamino)propanoate
https://huagongshe.com/reaction/588856
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 2-bromopropionate | HCID 95576 | — |
| Reactant | Tert-butyl 4-chloro-5-iodo-2-methoxybenzenamine | HCID 131734451 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 2-(4-chloro-5-iodo-2-methoxyphenylamino)propanoate | HCID 117610370 | 43% |
Reaction Steps
A mixture of tert-butyl 4-chloro-5-iodo-2-methoxybenzenamine (2 g, 7.07 mmol), methyl 2-bromopropanoate (1.17 g, 7.07 mmol), K2CO3 (1.94 g, 14.14 mmol) and KI (0.235 g, 1.414 mmol) in DMF (25 mL) was stirred at 100° C. for 16 h. The mixture was allowed to cool to RT, quenched with aqueous NaHCO3 solution and then extracted with ethyl acetate. The organic layer was washed with brine, dried over Na2SO4, filtered and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel (ethyl acetate/petroleum ether=1:20) to afford the desired product (1.12 g, 43% yield) as a yellow solid. ESI-MS m/z: 370.1[M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09227978B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-2e8e470483524951a5a5c8a6bedf958e |
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| Source note | uspto-grants-2016_01 |
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