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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 354302생성일: 2026년 10월 25일

Trifluoroacetic acid → dimethyl (S)-4-(2-pyrrolidinylmethoxy)isophthalate

https://huagongshe.com/reaction/354302

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참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물dimethyl (S)-4-[1-(tert-butoxycarbonyl)-2-pyrrolidinylmethoxy]isophthalateHCID 86595076—
용매DichloromethaneHCID 6344—
생성물dimethyl (S)-4-(2-pyrrolidinylmethoxy)isophthalateHCID 8659507253.4%

반응 단계

A mixture of dimethyl (S)-4-[1-(tert-butoxycarbonyl)-2-pyrrolidinylmethoxy]isophthalate (2.01 g, 5.11 mmol), TFA (20 mL), and CH2Cl2 (25 mL) was stirred for 1.5 hr at room temp. The resulting mixture was concentrated in vacuo and made basic with sat. NaHCO3. The mixture was extracted with CH2Cl2, washed with brine, dried over Na2CO3, and evaporated. The residue was purified by column chromatography on silica-gel with CHCl3—MeOH (9:1, v/v) as eluent to give 0.80 g (53%) dimethyl (S)4-(2-pyrrolidinylmethoxy)isophthalate as a yellow oil. 1H-NMR (CDCl3) δ1.71 (m, 1 H), 1.89 (m, 2 H), 2.00 (m, 1 H), 3.05-3.13 (m, 2 H), 3.67 (m, 1 H), 3.90 (s, 3 H), 3.91 (s, 3 H), 4.05-4.18 (m, 2H), 7.00 (d, 1 H, J=8.8 Hz), 8.14 (dd, 1 H, J=2.4, 8.8 Hz), 8.50 (d, 1 H, J=2.4 Hz).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06756378B2
출처 데이터셋uspto-grants-2004_06
ORD IDord-b92632aa88fa4a8593452c90b5d6b614
출처 메모uspto-grants-2004_06