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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 37358Erstellt: 25. Oktober 2026

Methyl Ethyl Ketone → 6-Bromo-3-pyridinemethanol

https://huagongshe.com/reaction/37358

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl Ethyl KetoneHCID 6569—
EduktSodium HydroxideHCID 14798—
EduktMethyl 6-bromopyridine-3-carboxylateHCID 13349623—
EduktDiisobutylaluminumhydrideHCID 21225700—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt6-Bromo-3-pyridinemethanolHCID 642124989,2%

Reaktionsschritte

To a mechanically-stirred solution of 80 g of methyl 6-bromo-nicotinate in a mixture of 386 mL of tetrahydrofuran and 114 mL of toluene at 0° C. was added drop by drop a 1.5 molar toluene solution of diisobutyl aluminium hydride at a rate such that the temperature never exceeded 10° C. This addition took 50 minutes. 21.59 mL of methyl ethyl ketone was added to the reaction mixture while the temperature rose to 25° C. A solution of 2.58 g of NaOH in 40 mL of water was added to the reaction mixture drop by drop (CAUTION: EXOTHERMIC). 121 mL of water was added with vigorous stirring. After completion of the addition, a white solid appeared. The mixture was filtered through celite and 196 mL of toluene was used to wash the solid and filter. The filtrate was concentrated in vacuo and 48 mL of heptane was added. The mixture was cooled in an ice-salt bath for 1 hour. The precipitated solid was filtered and washed with heptane to give 62.09 g of 3-hydroxymethyl-6-bromopyridine as a solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05420270
Quelldatensatzuspto-grants-1995_05
ORD IDord-c2b8b28ff16f4240bad50857a6e99962
Quellennotizuspto-grants-1995_05