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HRID 891951Erstellt: 26. Oktober 2026

Diiodomethane → 2-(3-Cyclopropylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

https://huagongshe.com/reaction/891951

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiiodomethaneHCID 6346—
EduktAmmonium ChlorideHCID 25517—
Edukt2-(3-Ethenylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 22240170—
EduktHCID 178418750HCID 178418750—
LösungsmittelTolueneHCID 1140—
Produkt2-(3-Cyclopropylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 2224022269%

Reaktionsschritte

To a solution of 4,4,5,5-tetramethyl-2-(3-vinyl-phenyl)-[1,3,2]dioxaborolane (300 mg, 1.3 mmol) in toluene (10 ml) were added diethylzinc solution (1.1 N in toluene, 5.22 ml, 5.74 mmol) and diiodomethane (8.7 ml, 33 mmol). The reaction mixture was stirred for 1 hour at room temperature and then refluxed for 3 hours. The reaction mixture was poured on sat. NH4Cl solution (20 ml) and was extracted with ethyl acetate. The combined organic layers were washed with brine, dried over MgSO4, filtered and concentrated in vacuo to provide 2-(3-cyclopropyl-phenyl)-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane (69% yield), 1H-NMR (300 MHz, CDCl3): δ=7.12-7.82 (m, 4H), 1.35 (s, 12H), 1.28 (t, 1H), 0.90-0.96 (m, 2H), 0.72-0.78 (m, 2H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07005432B2
Quelldatensatzuspto-grants-2006_02
ORD IDord-16faa739c8524138aadf0fb8526258e3
Quellennotizuspto-grants-2006_02