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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1955248Erstellt: 25. Oktober 2026

Triphenylphosphine → Methyl 5-(2-benzyloxy-ethoxy)-2-nitro-benzoate

https://huagongshe.com/reaction/1955248

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriphenylphosphineHCID 11776—
Edukt2-(Benzyloxy) ethanolHCID 12141—
EduktDiethyl azodicarboxylateHCID 5462977—
EduktMethyl 5-hydroxy-2-nitrobenzoateHCID 12922678—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktMethyl 5-(2-benzyloxy-ethoxy)-2-nitro-benzoateHCID 2329455293,1%

Reaktionsschritte

To a solution of methyl 5-hydroxy-2-nitro-benzoate (7.97 g, 40.43 mmol), triphenylphosphine (12.73 g, 48.53 mmol), and 2-benzyloxyethanol (5.86 ml, 41.24 mmol) in tetrahydofuran (100 ml) was added DEAD (8.04 ml, 95%, 48.51 mmol) dropwise. After addition of the DEAD, the reaction was stirred under nitrogen for 18 h. The solvent was evaporated, benzene was added, and the triphenylphosphine oxide was filtered off. The solid was washed with some benzene, and the filtrate evaporated. The yellow oil was dissolved in minimal benzene, and chromatographed on silica gel eluting with 25% ethyl acetate/hexanes to give methyl 5-(2-benzyloxy-ethoxy)-2-nitro-benzoate (12.47 g, 93%) as a light yellow oil. Analysis calculated for C17H17NO6 : C, 61.63; H, 5.17; N, 4.23. Found: C, 61.46; H, 5.02; N, 4.28.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06124323
Quelldatensatzuspto-grants-2000_09
ORD IDord-ac4f6ec9b9d94a3390bbbd2e71cdb15d
Quellennotizuspto-grants-2000_09