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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 78211Erstellt: 25. Oktober 2026

Dibromomethane → 2-(Bromomethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

https://huagongshe.com/reaction/78211

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDibromomethaneHCID 3024—
EduktMethanesulfonic AcidHCID 6395—
EduktPinacolHCID 6425—
EduktTriisopropyl borateHCID 21531—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-(Bromomethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 1095511068%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a mixture of triisopropyl borate (20 g, 110 mmol), dibromomethane (8.6 mL, 120 mmol), and tetrahydrofuran (150 mL) was added dropwise n-butyl lithium (2.6 M n-hexane solution, 39 mL, 100 mmol) over a period of 1.5 hours at −78° C., and then the reaction mixture was stirred for 1.5 hours at the same temperature. This mixture was then stirred for 2 hours at room temperature, after which it was cooled to 0° C., methanesulfonic acid (6.5 mL, 100 mmol) was added to the reaction mixture, and then the reaction mixture was stirred for 1 hour at room temperature. The mixture was cooled to 0° C., pinacol (12 g, 100 mmol) was added to the reaction mixture, and the reaction mixture was then stirred for 1 hour at room temperature. The reaction mixture was concentrated under a reduced pressure, after which the residue thus obtained was distilled under a reduced pressure (74-76° C., 8 mmHg) to obtain the title compound (16 g, 68%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08841327B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-66777c18e9f14f7ba638ae3747947439
Quellennotizuspto-grants-2014_09