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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1611901Erstellt: 25. Oktober 2026

Acetic Acid → 5-methylpentadecanoic Acid

https://huagongshe.com/reaction/1611901

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktBenzeneHCID 241—
EduktCarbon DioxideHCID 280—
EduktChloroacetateHCID 518964—
KatalysatorPalladiumHCID 23938—
Produkt5-methylpentadecanoic AcidHCID 9859906—

Reaktionsschritte

See GENERAL PROCEDURE I. Decyl bromide (compound (1), R═CH3(CH2)9—) is converted to its Grignard reagent with magnesium in dry ether (I, Step (a)). To this is added 5-chloro-2-pentanone (Aldrich C6,2660-3) (I, Step (b)). The reaction mixture is worked up with acetic anhydride (I, Step (c)) to form chloroacetate (3). Acetic acid is eliminated by refluxing (3) in a suitable solvent, e.g., benzene (I, Step (d)) yielding a mixture of chloro-olefin isomers (4). (4) is converted to its Grignard reagent following standard practice. (I, Step (e)). The Grignard reagent is treated with carbon dioxide and aqueous acidic workup (I, Step (f)) followed by catalytic hydrogenation (Pd catalyst) to form 5-methylpentadecanoic acid, (5).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06992057B2
Quelldatensatzuspto-grants-2006_01
ORD IDord-61eb50cd533b47c2b059d75dc6e994ed
Quellennotizuspto-grants-2006_01