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HRID 484357Erstellt: 24. Oktober 2026

Ethylparaben → Ethyl 4-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-2-naphthoyloxy)benzoate

https://huagongshe.com/de/reaction/484357

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthylparabenHCID 8434—
EduktDicyclohexylcarbodiimideHCID 10868—
Edukt5,5,8,8-Tetramethyl-5,6,7,8-tetrahydronaphthalene-2-carboxylic acidHCID 227638—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelDichloromethaneHCID 6344—
ProduktEthyl 4-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-2-naphthoyloxy)benzoateHCID 19748015—

Reaktionsschritte

A solution of 116 mg (0.5 mmol) of 5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-2-naphthoic acid, 58 mg (0.5 mmol) of ethyl 4-hydroxybenzoate, 117 mg (0.56 mmol) of 1,3-dicyclohexylcarbodiimide and 30 mg (0.25 mmol) of 4-dimethylaminopyridine in 15 ml of methylene chloride was stirred at room temperature for 12 hours. The reaction mixture was then filtered and the filtrate concentrated in-vacuo. The resultant residue was purified by flash chromatography (silica; 5% ethyl acetate in hexanes) to give the title compound as white crystals. PMR (CDCl3): δ 1.32 (6H, s), 1.36 (6H, s), 1.42 (3H, t, J~7.0 Hz), 1.73 (4H, s), 4.40 (2H, q, J~7.0 Hz), 7.28 (2H, d, J~8.1 Hz), 7.45 (1H, d, J~8.8 Hz), 7.93 (1H, dd, J~8.8 Hz, 1.8 Hz), 8.13 (2H, d, J~8.1 Hz), 8.14 (1H, s).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05231113
Quelldatensatzuspto-grants-1993_07
ORD IDord-0af8ec32ede14ba190806974841680ca
Quellennotizuspto-grants-1993_07