HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 880145Generated: November 1, 2026
Cyclopropylboronic acid → 3-Cyclopropyl-4-fluoroaniline
https://huagongshe.com/reaction/880145
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclopropylboronic acid | HCID 2760897 | — |
| Reactant | 3-Bromo-4-fluoroaniline | HCID 2779286 | — |
| Reactant | HCID 178527066 | HCID 178527066 | — |
| Catalyst | Tricyclohexylphosphine | HCID 75806 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-Cyclopropyl-4-fluoroaniline | HCID 57416303 | 65.4% |
Reaction Steps
558 mg of cyclopropylboronic acid, 3.7 g of tribasic potassium phosphonate, 70 mg of tricyclohexylphosphane and 56 mg of palladium(2+) diacetate in 1.5 ml of water are added to a solution of 950 mg of 3-bromo-4-fluoroaniline in 20 ml of toluene, with stirring and under argon. The mixture is degassed and then heated to a temperature of 100° C. After 15 hours, the reaction medium is cooled to a temperature in the region of 20° C., run into 100 ml of water, and then extracted with four times 60 ml of diethyl ether. The combined organic phases are dried over anhydrous magnesium sulphate, filtered and concentrated under reduced pressure. The residue is purified on a silica column, eluent: 7030 cyclohexaneethyl acetate. 494 mg of 3-cyclopropyl-4-fluoroaniline are obtained in the form of a brown oil, the characteristics of which are the following:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08993565B2 |
|---|
| Source dataset | uspto-grants-2015_03 |
|---|
| ORD ID | ord-af0b169222ca4ed9bbeb016d1134a47c |
|---|
| Source note | uspto-grants-2015_03 |
|---|