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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 30484생성일: 2026년 10월 24일

Triphenylphosphine → 3-(3-Piperidin-1-yl-propoxy)-isoxazole-5-carboxylic acid methyl ester

https://huagongshe.com/ko/reaction/30484

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물Piperidine-1-propanolHCID 66032—
반응물Di-tert-butyl azodicarboxylateHCID 97268—
반응물HCID 178498603HCID 178498603—
용매DichloromethaneHCID 6344—
생성물3-(3-Piperidin-1-yl-propoxy)-isoxazole-5-carboxylic acid methyl esterHCID 44515459192.6%

반응 단계

3-Hydroxy-isoxazole-5-carboxylic acid methyl ester (0.859 g., 6.00 mmol) and 3-piperidin-1-yl-propan-1-ol (0.860 g., 6.00 mmol) were dissolved in DCM (30 mL), and polymer-supported Ph3P resin (3 mmol/g, 3.1 g, 9.30 mmol) was added. The mixture was stirred for 10 min and di-tert-butyl azodicarboxylate (2.14 g, 9.30 mmol) was then added. The reaction mixture was stirred under nitrogen for 18 h. The reaction was quenched with 1 N NaOH (20 mL) and was stirred for 30 min. The resulting mixture was extracted with DCM (3×30 mL). The combined organic extracts were dried over Na2SO4, filtered, and concentrated to yield a crude oily product (3.1 g), which was purified (SiO2: 5% 2 M NH3 in MeOH/DCM) to yield the title compound (0.88 g, 58%). MS (ESI): exact mass calcd. for C13H20N2O4, 268.14; m/z found, 269.4 [M+H]+. 1H NMR (500 MHz, CDCl3): 6.53 (s, 1H), 4.34-4.30 (m, 2H), 3.94 (s, 3H), 2.47-2.34 ( 6H), 2.02-1.94 (m, 2H), 1.61-1.54 (m, 4H), 1.47-1.39 (m, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07423147B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-546ba2e9a0d44059960235eb0d1660a1
출처 메모uspto-grants-2008_09