HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1802336Generated: October 25, 2026
Potassium Phosphate, Tribasic → 3-Cyclopropyl-4-methoxybenzonitrile
https://huagongshe.com/reaction/1802336
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | Tricyclohexylphosphine | HCID 75806 | — |
| Reactant | 3-Bromo-4-methoxybenzonitrile | HCID 736049 | — |
| Reactant | Cyclopropylboronic acid | HCID 2760897 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-Cyclopropyl-4-methoxybenzonitrile | HCID 57484707 | — |
Reaction Steps
A mixture of 3-bromo-4-methoxybenzonitrile (2-1, 5.0 g, 23.6 mmol, 1.0 eq), aqueous potassium phosphate tribasic (65.0 ml, 1.27 M, 3.5 eq), cyclopropylboronic acid (10.1 g, 118 mmol, 5.0 eq), Pd(OAc)2 (0.539 g, 2.36 mmol, 0.1 eq) and tricyclohexylphosphine (0.661 g, 2.36 mmol, 0.1 eq) was stirred in degassed toluene (103 ml) and heated to 80° C. for three hours. An additional amount of cyclopropylboronic acid (1.0 g, 1.16 mmol, 0.5 eq) was added and the solution was further heated for 16 hours at 80° C. to complete the reaction. The reaction mixture was cooled and partitioned between brine and EtOAc. The organic phase was dried over sodium sulfate, filtered and concentrated to give an orange oil. The oil was purified by normal phase column chromatography (0 to 10% EtOAc in hexanes) to afford the product (2-2) as a yellow oil. 1H NMR (CDCl3) δ 7.44 (dd, 1H, J=8.4, 2.0 Hz), 7.09 (d, 1H, J=2.0 Hz), 6.86 (d, 1H, J=8.4 Hz), 3.92 (s, 3H), 2.13 (m, 1H), 0.97 (m, 2H), 0.65 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08349872B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-689d1f1932e3475180e0b19bdc0b1afd |
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| Source note | uspto-grants-2013_01 |
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