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HRID 1091008Erstellt: 26. Oktober 2026

Tributyl phosphite → 7-[(Phenoxyacetyl)amino]-8-oxo-3-(dibutoxyphosphinyl)-1-azabicyclo[4.2.0]-oct-2-ene-2-carboxylic acid (diphenylmethyl)ester

https://huagongshe.com/reaction/1091008

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTributyl phosphiteHCID 7623—
Edukt3-Bromo-7-[(phenoxyacetyl)amino]-8-oxo-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid (diphenylmethyl)esterHCID 54021189—
KatalysatorNickel DichlorideHCID 24385—
LösungsmittelTolueneHCID 1140—
Produkt7-[(Phenoxyacetyl)amino]-8-oxo-3-(dibutoxyphosphinyl)-1-azabicyclo[4.2.0]-oct-2-ene-2-carboxylic acid (diphenylmethyl)esterHCID 5443562424%

Reaktionsschritte

A solution of 3-bromo-7-[(phenoxyacetyl)amino]-8-oxo-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid (diphenylmethyl)ester (2 g, 3.6 mmol) in toluene (50 mL) was added tri-n-butyl phosphite (15 mL) and nickel(II)chloride (50 mg, 039 mmol). The reaction was brought to reflux under nitrogen. Each hour, the reaction was cooled and an additional portion of nickel(II)chloride (50 mg, 0.39 mmol) was added. This process was continued for a total of six hours. The reaction was concentrated in vacuo and the residue purified by flash chromatography on silica gel (25%-50% ethyl acetate/hexanes) to provide 7-[(Phenoxyacetyl)amino]-8-oxo-3-(dibutoxyphosphinyl)-1-azabicyclo[4.2.0]-oct-2-ene-2-carboxylic acid (diphenylmethyl)ester (588 mg, 24%):

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05084447
Quelldatensatzuspto-grants-1992_01
ORD IDord-d19399c0952d478e8702ac24718e13f3
Quellennotizuspto-grants-1992_01