HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1270734Generated: November 2, 2026
Potassium Phosphate, Tribasic → 2-Chloro-4-cyclopropyl-5-methyl-6-fluoroaniline
https://huagongshe.com/reaction/1270734
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | Tricyclohexylphosphine | HCID 75806 | — |
| Reactant | Cyclopropylboronic acid | HCID 2760897 | — |
| Reactant | 2-Chloro-4-bromo-5-methyl-6-fluoroaniline | HCID 18451500 | — |
| Solvent | Water 1,2-dimethoxyethane | HCID 18180031 | — |
| Product | 2-Chloro-4-cyclopropyl-5-methyl-6-fluoroaniline | HCID 18451503 | — |
Reaction Steps
2-Chloro-4-bromo-5-methyl-6-fluoroaniline (6.5 g, 27 mmol), cyclopropylboronic acid (2.8 g, 33 mmol), tetrakis (triphenylphosphine)palladium (0) (1.4 g, 1.3 mmol), potassium phosphate (20.2 g, 95 mmol) and tricyclohexylphosphine (0.77 g, 2.7 mmol) are combined and stirred in 200 mL of a 4:1 DME/water solution. The mixture is degassed by repeated alternating application of vacuum and positive nitrogen pressure (10×). The mixture is heated to reflux temperature for 2 days and then cooled to room temperature. Most of the DME is removed by rotary evaporator and the residual mixture is partitioned between Et2O (250 mL) and water (250 mL). The organic phase is washed with brine (3×250 mL), dried (MgSO4) and concentrated by rotary evaporator. The crude product is purified using flash chromatography (8% CH2Cl2/hexanes) to give 2-chloro-4-cyclopropyl-5-methyl-6-fluoroaniline as a tan oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07202364B2 |
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| Source dataset | uspto-grants-2007_04 |
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| ORD ID | ord-2baa8c18e5704287afaadc91bd50569f |
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| Source note | uspto-grants-2007_04 |
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