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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 560951Erstellt: 24. Oktober 2026

11-Bromoundecanoic acid → N3(CH2)10C(O)Cl

https://huagongshe.com/de/reaction/560951

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt11-Bromoundecanoic acidHCID 17812—
EduktSodium AzideHCID 33557—
EduktOxalyl chlorideHCID 65578—
Edukt11-Azidoundecanoic acidHCID 454094—
LösungsmittelBenzeneHCID 241—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelSodium chloride; waterHCID 57417360—
ProduktN3(CH2)10C(O)ClHCID 22283452—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

In a glass reaction vessel, 10.6 grams (40 mmol) of 11-Bromoundecanoic acid was dissolved in 225 milliliters DMF and 26 grams (400 mmol) sodium azide was added. The resulting stirred mixture was heated to 80° C. for 16 h, and then the reaction mixture was worked up with ether and brine. The ether layer was dried (MgSO4), filtered, and concentrated to 9.5 grams of N3(CH2)10C(O)OH as a pale yellow oil which was used without purification. In a glass reaction vessel, the N3(CH2)10C(O)OH was dissolved in 120 milliliters benzene and 12.7 grams (100 mmol) oxalyl chloride was added. The reaction was allowed to stir for 20 h, at which time the volatiles were removed in vacuo. The resulting residue was dissolved in pentane and filtered in a nitrogen atmosphere to remove solids. Concentration of the filtrate afforded N3(CH2)10C(O)Cl as a clear, yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08063164B2
Quelldatensatzuspto-grants-2011_11
ORD IDord-1517c54aba0f452892d62f89cf8b329f
Quellennotizuspto-grants-2011_11