Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1374076Erstellt: 24. Oktober 2026

Triethylamine → (3-Bromo-2-oxo-piperidin-1-yl)acetic acid benzyl ester

https://huagongshe.com/de/reaction/1374076

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktSodium HydroxideHCID 14798—
EduktO-benzylglycine toluene-p-sulphonateHCID 6451311—
Edukt1-Butanaminium, N,N,N-tributyl-, carbonic acid (1:1)HCID 11012140—
Edukt41339-29-1HCID 11185032—
LösungsmittelDichloromethaneHCID 6344—
Produkt(3-Bromo-2-oxo-piperidin-1-yl)acetic acid benzyl esterHCID 69484297—

Reaktionsschritte

67.7 g (0.2 mol) of glycine benzyl ester tosylate and 61.2 ml (0.44 mol) of triethylamine are dissolved in 200 ml of methylene chloride and added in drops at 0° C. to a solution of 55.7 g (0.2 mol) of 2,5-dibromovaleric acid chloride (Okawara et al. Chem. Pharm. Bull. (1982), (30), 1225) in 200 ml of methylene chloride within 45 minutes, and it is stirred for 18 hours at room temperature. The reaction mixture is now added in drops at 0° C. to a solution of 400 ml of aqueous 32% sodium hydroxide and 2 g of tetrabutylammonium hydrogen carbonate (about 15 minutes), and it is stirred for 30 minutes. Then, the phases are separated, and the aqueous phase is extracted three times with 200 ml of dichloromethane each. The organic phases are dried on sodium sulfate, the solution is evaporated to the dry state and chromatographed on silica gel (methylene chloride). The fractions that contain the product are combined and concentrated by evaporation.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07164016B2
Quelldatensatzuspto-grants-2007_01
ORD IDord-9da6f88e5c9d425f975ad89bb11f4551
Quellennotizuspto-grants-2007_01