HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705370Generated: October 30, 2026
Potassium Phosphate, Tribasic → 4-Chloro-2-cyclopropyl-5-methoxyaniline
https://huagongshe.com/reaction/705370
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | Tricyclohexylphosphine | HCID 75806 | — |
| Reactant | Cyclopropylboronic acid | HCID 2760897 | — |
| Reactant | 2-Bromo-4-chloro-5-methoxyaniline | HCID 14774783 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-Chloro-2-cyclopropyl-5-methoxyaniline | HCID 67981800 | — |
Reaction Steps
A mixture of Example 18A (1.0 equivalents), cyclopropyl boronic acid (1.1 equivalents), tricyclohexylphosphine (0.05 equivalents), palladium acetate (0.025 equivalents) and K3PO4 (2 equivalents) in a 20:1 volume ratio of toluene and water was sparged with nitrogen for 15 minutes. The reaction mixture was then heated to 100° C. for 12 hours, cooled, diluted with water, stirred for 1 hour and filtered through a diatomaceous earth pad, and the pad was rinsed with toluene. The filtrate was mixed and the layers were separated. The organic layer was washed with water and saturated brine, dried (Na2SO4), filtered and concentrated to an oil that was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09173887B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-16c24fb3fd994b17a23e486d2fc38b36 |
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| Source note | uspto-grants-2015_11 |
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