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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1913956Erstellt: 26. Oktober 2026

Triethylamine → (S,E)-N-(8-(tert-Butyldiphenylsilyloxy)-2-methyloct-5-en-4-yl)-P,P-diphenylphosphinic amide

https://huagongshe.com/reaction/1913956

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktDiphenylphosphinic chlorideHCID 73910—
Edukt(S,E)-8-(tert-Butyldiphenylsilyloxy)-2-methyloct-5-en-4-amine hydrochlorideHCID 53248329—
LösungsmittelHydrochloric AcidHCID 313—
LösungsmittelDichloromethaneHCID 6344—
Produkt(S,E)-N-(8-(tert-Butyldiphenylsilyloxy)-2-methyloct-5-en-4-yl)-P,P-diphenylphosphinic amideHCID 67310501119,6%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of the amine 7 (400 mg, 1.01 mmol) in dry DCM (7 mL) were added Et3N (0.44 mL, 3.13 mmol), and then a solution of diphenylphosphinic chloride (Ph2POCl, 0.22 mL, 1.11 mmol) in dry DCM (3 mL) at 0° C. After being stirred at 0° C. for 15 min, the reaction mixture was allowed to warm to rt and stirred for 4 h, then diluted with DCM and 10% HCl. The aqueous phase was extracted with DCM and the combined organic layers were washed with sat. NaHCO3, dried (MgSO4), filtered and concentrated in vacuo to afford 720 mg of the crude title compound as a pale yellow solidified oil, which was used for the next step without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08609850B2
Quelldatensatzuspto-grants-2013_12
ORD IDord-14f3519a12fe4c7e973c844e1fc5462e
Quellennotizuspto-grants-2013_12