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HRID 447487Erstellt: 26. Oktober 2026
4,4,5,5-Tetramethyl[1,3,2]dioxaborolane → (E)-N,N-dimethyl-1-(4-(2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)vinyl)phenyl)methanamine
https://huagongshe.com/reaction/447487
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 4,4,5,5-Tetramethyl[1,3,2]dioxaborolane | HCID 2734768 | — |
| Edukt | 1-(4-ethynylphenyl)-N,N-dimethylmethanamine | HCID 86658829 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | (E)-N,N-dimethyl-1-(4-(2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)vinyl)phenyl)methanamine | HCID 58486139 | 84,8% |
Reaktionsschritte
4,4,5,5-Tetramethyl-1,3,2-dioxaborolane (1.20 mL, 8.23 mmol) was added to an argon-purged solution of 1-(4-ethynylphenyl)-N,N-dimethylmethanamine (262 mg, 1.65 mmol) and HRuCl(CO)(PPh3)3 (104.1 mg, 0.11 mmol) in toluene (9.0 mL). The resulting mixture was heated at 50° C. for 12 h. The product was extracted into Et2O (250 mL), and the organic layer was washed sequentially with water (3×20 mL) and brine (20 mL), dried (Na2SO4) and evaporated in vacuo. Purification by column chromatography (silica gel, 50-100% CH2Cl2 in Et2O) gave (E)-N,N-dimethyl-1-(4-(2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)vinyl)phenyl)methanamine (402 mg, containing 20% pinacol impurity by 1H NMR, 68% yield). 1H NMR (400 MHz, CDCl3) δ 7.46 (d, J=8 Hz, 2H), 7.4 (d, 1H), 7.28 (d, 2H), 6.16 (d, 1H), 3.42 (s, 2H), 2.24 (s, 6H), 1.32 (s, 12H); MS ESI 288.0 [M+H]+, calcd for [C17H26BNO2+H]+ 288.2.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08481525B2 |
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| Quelldatensatz | uspto-grants-2013_07 |
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| ORD ID | ord-04846c1b37914cfbb37ffc746b9cf497 |
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| Quellennotiz | uspto-grants-2013_07 |
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