HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2173131Generated: October 30, 2026
Potassium Phosphate, Tribasic → HCID 86692999, compound
https://huagongshe.com/reaction/2173131
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | Tricyclohexylphosphine | HCID 75806 | — |
| Reactant | Cyclopropylboronic acid | HCID 2760897 | — |
| Reactant | HCID 67517481 | HCID 67517481 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 86692999 | HCID 86692999 | — |
Reaction Steps
To a microwave tube charged with tert-butyl-4-[2-(4-iodo-1-oxo-1,3-dihydro-2-benzofuran-5-yl)ethyl]piperazine-1-carboxylate (100 mg, 0.21 mmol) and a stir bar was added palladium acetate (3.6 mg, 0.016 mmol), tricyclohexylphosphine (8.9 mg, 0.032 mmol), cyclopropyl boronic acid (27 mg, 0.32 mmol), and potassium phosphate (160 mg, 0.74 mmol). The tube was sealed, and injected toluene (2 mL) and water (100 uL). The mixture was purged three times with nitrogen, and heated to 100° C. for 30 minutes. LC showed formation of the desired product. The reaction was purified by silica gel chromatography to afford tert-butyl-4-[2-(4-cyclopropyl-1-oxo-1,3-dihydro-2-benzofuran-5-yl)ethyl]piperazine-1-carboxylate. LC-MS (IE, m/z): 387 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09056859B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-41cac634a4804f57a9f943f9b6a16381 |
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| Source note | uspto-grants-2015_06 |
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