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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1169335Erstellt: 27. Oktober 2026

Triphenylphosphine → methyl 2-(4-ethoxybenzyloxy)-6,7-dihydro-5H-benzocycloheptene-8-carboxylate

https://huagongshe.com/reaction/1169335

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriphenylphosphineHCID 11776—
EduktDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Edukt4-Ethoxybenzyl alcoholHCID 80345—
Eduktmethyl 2-hydroxy-6,7-dihydro-5H-benzocycloheptene-8-carboxylateHCID 22989944—
LösungsmittelTetrahydrofuranHCID 8028—
Produktmethyl 2-(4-ethoxybenzyloxy)-6,7-dihydro-5H-benzocycloheptene-8-carboxylateHCID 2299016858%

Reaktionsschritte

To triphenylphosphine (590 mg, 2.25 mmol), 4-ethoxybenzyl alcohol (342 mg, 2.25 mmol) and methyl 2-hydroxy-6,7-dihydro-5H-benzocycloheptene-8-carboxylate (327 mg, 1.50 mmol) dissolved in THF (6 ml) was added at 0° C. a solution of diisopropyl azodicarboxylate (0.439 ml, 2.23 mmol) in THF (2 ml), and the resulting mixture was stirred at room temperature for 6 hours. The reaction mixture was concentrated under reduced pressure and the residue was subjected to column chromatography (silica gel: 50 g, ethyl acetate/hexane=1/25→1/19). The objective fractions were concentrated under reduced pressure, diisopropyl ether was added to the residue and an insoluble material was collected by filtration. The insoluble material was washed with diisopropyl ether and was then dried under reduced pressure to obtain methyl 2-(4-ethoxybenzyloxy)-6,7-dihydro-5H-benzocycloheptene-8-carboxylate (308 mg, 0.87 mmol, 58%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06627651B1
Quelldatensatzuspto-grants-2003_09
ORD IDord-46a33065fd3244839a5147be87fb6861
Quellennotizuspto-grants-2003_09