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HRID 1004491Erstellt: 23. Oktober 2026

Trimethylboroxine → (3aS)-1-methyl-3,3-diphenyl-hexahydropyrrolo(1,2-c)(1,3,2)oxazaborole

https://huagongshe.com/de/reaction/1004491

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrimethylboroxineHCID 574072—
Edukt2-Pyrrolidinemethanol, alpha,alpha-diphenyl-, (S)-HCID 2724899—
LösungsmittelTolueneHCID 1140—
Produkt(3aS)-1-methyl-3,3-diphenyl-hexahydropyrrolo(1,2-c)(1,3,2)oxazaboroleHCID 2734713100%

Reaktionsschritte

Under argon stream, to a solution of (S)-α,α-diphenyl-2-pyrrolidine methanol (3 g, 11.8 mmol) in dry toluene (90 ml) was added trimethyl boroxine (1.13 ml, 8.0 mmol), followed by stirring for 1.5 hours. After the argon stream was stopped and the toluene (22.5 ml) was recovered under normal pressures on an oil bath at 140° C., dry toluene (22.5 ml) was added. Furthermore, after this recovery operation was repeated twice, the resultant product was concentrated under normal pressures, and subsequently under a reduced pressure, to thereby obtain the titled compound as a colorless crystalline.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06049009
Quelldatensatzuspto-grants-2000_04
ORD IDord-4a63ecdf7488425e96ba5e72240b0c99
Quellennotizuspto-grants-2000_04