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HRID 24018Erstellt: 23. Oktober 2026

Triethylamine → Naphthalene-2-yl-propynoic acid ethyl ester

https://huagongshe.com/de/reaction/24018

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktTriphenylphosphine OxideHCID 13097—
EduktTrifluoromethanesulfonic anhydrideHCID 67749—
Edukt3-Naphthalen-2-yl-3-oxopropionic acid ethyl esterHCID 2760158—
Lösungsmittel1,2-DichloroethaneHCID 11—
ProduktNaphthalene-2-yl-propynoic acid ethyl esterHCID 6681901642,7%

Reaktionsschritte

Triflic anhydride (2.9 mL, 17 mmol) was added dropwise to a solution of triphenylphosphine oxide (4.8 g, 17 mmol) in 1,2-dichloroethane (40 mL) at 0° C. The resulting suspension was stirred for 15 minutes, followed by the dropwise addition of a solution of 3-naphthalen-2-yl-3-oxo-propionic acid ethyl ester (3.2 g, 12 mmol) in 1,2-dichloroethane (40 mL). After the addition was complete, triethylamine (4.0 mL, 29 mmol) was added and the reaction mixture was heated at reflux for 1 hr. The solution was cooled to room temperature, washed with water, and dried (MgSO4). The solvent was removed under reduced pressure, and the product was purified via column chromatography with silica eluting with hexane/ethyl acetate (9/1) to yield naphthalene-2-yl-propynoic acid ethyl ester (1.15 g, 37% yield) as a yellow oil. 1H NMR (CDCl3) δ 8.25 (s, 1H), 7.95 (m, 3H), 7.66 (m, 3H), 4.46 (m, 2H), 1.51 (t, 3H, J=8.0 Hz).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06855722B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-31126ea1635145a9b5623050008ac4fc
Quellennotizuspto-grants-2005_02