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HRID 24018作成日:2026年10月25日

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

https://huagongshe.com/reaction/24018

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Triphenylphosphine OxideHCID 13097—
反応物Trifluoromethanesulfonic anhydrideHCID 67749—
反応物3-Naphthalen-2-yl-3-oxopropionic acid ethyl esterHCID 2760158—
溶媒1,2-DichloroethaneHCID 11—
生成物Naphthalene-2-yl-propynoic acid ethyl esterHCID 6681901642.7%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06855722B2
出典データセットuspto-grants-2005_02
ORD IDord-31126ea1635145a9b5623050008ac4fc
出典メモuspto-grants-2005_02