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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 414933생성일: 2026년 10월 24일

2-Methyl-2-nitro-1,3-propanediol → HCID 21075963, 화합물

https://huagongshe.com/ko/reaction/414933

반응식

참여 물질

역할이름HCID투입량
반응물2-Methyl-2-nitro-1,3-propanediolHCID 6480—
반응물DicyclohexylcarbodiimideHCID 10868—
반응물NaproxenHCID 156391—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물HCID 21075963HCID 21075963—

반응 단계

A solution of 1,3-dicyclohexylcarbodiimide (4.23 g, 20.5 mmol), (2S)-2-(6-methoxy(2-naphthyl))propanoic acid (naproxen, 4.34 g, 18.9 mmol), and 2-nitro-2-methyl-1,3-propanediol (2.56 g, 19.0 mmol) in CH2Cl2 (50 mL) and THF (50 mL) was stirred at ambient temperature overnight. The solvent was evaporated and EtOAc (100 mL) was added to the resulting crude material, cooled in a dry-ice bath and the byproduct, dicyclohexyl urea was removed by filtration. The product was separated by silica gel column chromatography eluting with ethyl acetate/hexane (1:3, Rf=0.1) to give the title compound (a mixture of diasteromers) as an oil (2.77 g, 42% yield). 1H NMR (300 MHz, CDCl3) δ 7.69-7.60 (m, 3H), 7.34-7.3 (m, 1H), 7.14-7.08 (m, 2H), 4.44 (d, J=4.2 Hz, 2H), 3.86 (s, 3H), 3.85 (q, J=7.2 Hz, 1H), 1.55 (d, J=7.2 Hz, 3H), 1.36 & 1.40 (s, 3H). 13C NMR (75 MHz, CDCl3) δ 174.14, 174.02 157.57, 134.53, 134.51, 133.64, 129.13, 128.7, 127.17, 125.87, 125.84, 119.0, 105.47, 89.53, 89.42, 64.67, 64.52, 64.19, 55.12, 45.04, 18.25, 18.03, 17.82, 17.79. Mass spectrum (API-TIS) m/z 348 (MH)−.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08088762B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-a46a86893bbe455788439d9b03e756a3
출처 메모uspto-grants-2012_01