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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 501707생성일: 2026년 10월 24일

Water → (S)-2,2,2-trifluoro-N-(6-methoxy-3-methylene-2,3-dihydro-1H-inden-1-yl)-acetamide

https://huagongshe.com/ko/reaction/501707

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물(S)-2,2,2-trifluoro-N-(6-methoxy-3-oxo-2,3-dihydro-1H-inden-1-yl)acetamideHCID 1472787—
반응물Potassium tert-butoxideHCID 23665647—
촉매Methyltriphenyliphosphonium bromideHCID 74505—
용매TetrahydrofuranHCID 8028—
생성물(S)-2,2,2-trifluoro-N-(6-methoxy-3-methylene-2,3-dihydro-1H-inden-1-yl)-acetamideHCID 8662233892.7%

반응 단계

Step AF (2): To a solution of methyltriphenylphosphonium bromide (1.6 g) in THF (5 mL) was added potassium t-butoxide (700 mg), and the mixture was stirred at rt for 30 min to form a deep yellow solution. A solution of (S)-2,2,2-trifluoro-N-(6-methoxy-3-oxo-2,3-dihydro-1H-inden-1-yl)acetamide (500 mg) in THF (2 mL) was added, and the reaction was continued for 40 min. Water was added, the aqueous layer was extracted with EtOAc (×3), and the combined organic layers were washed with brine, dried over anhydrous sodium sulfate, and filtered. The filtrate was evaporated in vacuo, and the residue was purified by Biotage chromatography eluting with 1-10% EtOAc/hexanes to give (S)-2,2,2-trifluoro-N-(6-methoxy-3-methylene-2,3-dihydro-1H-inden-1-yl)-acetamide as a white solid (460 mg). 1H NMR (400 MHz, CDCl3) δ 7.45 (1H, d), 6.91 (1H, dd), 6.83 (1H, d), 6.45 (1H, br. S), 5.38 (1H, dt), 5.38 (1H, t), 4.99 (1H, t), 3.81 (3H, s), 3.45 (1H, m), and 2.62 (1H, m).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07772221B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-80f83f9a40084def86405aa8dd3ec3ad
출처 메모uspto-grants-2010_08