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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1295157생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1295157

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Triphenylphosphine OxideHCID 13097—
반응물Trifluoromethanesulfonic anhydrideHCID 67749—
반응물3-Naphthalen-2-yl-3-oxopropionic acid ethyl esterHCID 2760158—
용매1,2-DichloroethaneHCID 11—
생성물Naphthalene-2-yl-propynoic acid ethyl esterHCID 6681901642.7%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07241789B2
출처 데이터셋uspto-grants-2007_07
ORD IDord-58bfc8e02dab4185bdaec5edd7e44d1c
출처 메모uspto-grants-2007_07