HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844250Generated: November 2, 2026
Potassium Carbonate → HCID 52920397, compound
https://huagongshe.com/reaction/1844250
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-(Trifluoromethyl)phenylboronic acid | HCID 2734388 | — |
| Reactant | HCID 67114629 | HCID 67114629 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Acetonitrile--water (1/1) | HCID 18373917 | — |
| Product | HCID 52920397 | HCID 52920397 | 80.8% |
Reaction Steps
A solution of 2-((trans)-2-(4-bromophenyl)cyclopropylamino)acetamide (100 mg, 0.37 mmol, 1 equiv), 3-trifluoro methyl benzene boronic acid (84 mg, 0.44 mmol 1.2 equiv), K2CO3 (152 mg, 1.11 mmol, 3 equiv) in CH3CN+H2O (4:1) (2 mL) was degassed for 30 min with Argon gas, then Pd(PPh3)4 (0.1 equiv) was added and the reaction mixture was heated at reflux temp. for 2 h. After completion, the reaction mixture was poured into ice water (10 mL), extracted with EtOAc (2×10 mL). The combined extracts were washed with water (10 mL), brine (10 mL), dried over anhydrous Na2SO4, filtered and evaporated. The crude residue was purified by prep HPLC to give 2-((trans)-2-(3′-(trifluoromethyl)biphenyl-4-yl)cyclopropylamino)acetamide (100 mg, 80% yield) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08946296B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-97f7939666d24dd384039b13d74855c4 |
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| Source note | uspto-grants-2015_02 |
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