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HRID 129250Erstellt: 25. Oktober 2026

Benzene → Methyl 4-[1-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthalenyl)-1-ethenyl]benzoate

https://huagongshe.com/reaction/129250

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzeneHCID 241—
EduktTolueneHCID 1140—
EduktSodium BicarbonateHCID 516892—
EduktPotassium bis(trimethylsilyl)amideHCID 3251421—
EduktMethyl 4-[(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-2-naphthyl)carbonyl]benzoateHCID 10784070—
KatalysatorMethyltriphenyliphosphonium bromideHCID 74505—
LösungsmittelMethylenechloride HexaneHCID 21226440—
ProduktMethyl 4-[1-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthalenyl)-1-ethenyl]benzoateHCID 999791180%

Reaktionsschritte

To a suspension of methyltriphenylphosphonium bromide (0.78 g, 2.18 mmol) in 5 mL of benzene under argon at room temperature was added a 0.5M solution of potassium hexamethyldisilazide in toluene (4.4 mL, 2.2 mmol), and the yellow solution was stirred for 5 min. A solution of keto-ester 3 (0.51 g, 1.455 mmol) in 7 mL of benzene was added, and the orange solution was stirred for 1 h at room temperature. The reaction mixture was poured into saturated aqueous NaHCO3 and extracted with 40% ethyl acetate/hexane. The combined organic layers were dried over anhydrous MgSO4, filtered through a plug of silica gel, and concentrated to afford a solid. Flash chromatography (30% dichloromethane/hexane) yielded the desired product 16 as a white solid (0.405 g, 80%): m.p. 117°-118° C.; Rf 0.2 (25% CH2Cl2 /hexane). The structure of the product was also confirmed using IR, 1H NMR and mass spectroscopy.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05466861
Quelldatensatzuspto-grants-1995_11
ORD IDord-71076597244a4d728395553e1843a512
Quellennotizuspto-grants-1995_11