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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295157Generated: October 25, 2026

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

https://huagongshe.com/reaction/1295157

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTriphenylphosphine OxideHCID 13097—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
Reactant3-Naphthalen-2-yl-3-oxopropionic acid ethyl esterHCID 2760158—
Solvent1,2-DichloroethaneHCID 11—
ProductNaphthalene-2-yl-propynoic acid ethyl esterHCID 6681901642.7%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07241789B2
Source datasetuspto-grants-2007_07
ORD IDord-58bfc8e02dab4185bdaec5edd7e44d1c
Source noteuspto-grants-2007_07