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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 425266Erstellt: 27. Oktober 2026

Acetic Acid → Borane;2-methylpyridine

https://huagongshe.com/reaction/425266

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktBoraneHCID 6331—
Edukt3-MethylpyridineHCID 7970—
Edukt4-EthylpyridineHCID 10822—
Edukt3-EthylpyridineHCID 10823—
Edukt2-PropylpyridineHCID 69320—
EduktBorane;pyridineHCID 2723995—
LösungsmittelPyridineHCID 1049—
ProduktBorane;2-methylpyridineHCID 16217944—
ProduktHCID 178419164HCID 178419164—
ProduktHCID 178419168HCID 178419168—
ProduktHCID 178419174HCID 178419174—

Reaktionsschritte

Pyridine forms an amine borane that is not moisture sensitive and very useful for reductive aminations and reductions in protic media. Pyridine borane is commercially available and often used in acetic acid to increase the reactivity of the borane. Unfortunately, it is thermally unstable and must be kept at temperatures less than 54° C. to avoid decomposition via hydroboration/polymerization processes. Its shelf-life at ambient temperature is only 6 months, Borane complexes of pyridine, 2-n-propylpyridine, 3-methylpyridine, 3-ethylpyridine and 4-ethylpyridine are liquids which violently decompose upon distillation (Mooney E. F. et al., J. Inorg. Nucl. Chem 1968, 30, p. 1439). 2-Picoline borane (mp. 50° C.), 2-ethylpyridine borane (mp, 50-51° C.), 2,6-lutidine borane (mp. 106-107° C.) and 2,4,6-collidine borane (mp. 99-100° C.) have been isolated as solids.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08106200B2
Quelldatensatzuspto-grants-2012_01
ORD IDord-4d143ad01d254d1b85140b1240a70419
Quellennotizuspto-grants-2012_01