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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 132618생성일: 2026년 10월 26일

Methyl iodide → (R)-3-((2R,3R)-2,3-Dimethyl-hexanoyl)-4-phenyl-oxazolidin-2-one

https://huagongshe.com/reaction/132618

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물SodiumHCID 5360545—
반응물(R)-3-((R)-3-Methyl-hexanoyl)-4-phenyl-oxazolidin-2-oneHCID 68955002—
용매TetrahydrofuranHCID 8028—
생성물(R)-3-((2R,3R)-2,3-Dimethyl-hexanoyl)-4-phenyl-oxazolidin-2-oneHCID 6919126356.5%

반응 조건

온도-78 °C

반응 단계

To a 1M THF solution of Sodium hexamethyldisylamide (16.2 g, 88.3 mmol) at −78° C. was added via canular a 0° C. solution of (R)-3-((R)-3-methyl-hexanoyl)-4-phenyl-oxazolidin-2-one (18.7 g, 67.9 mmol) in 70 mL dry THF. The resulting solution was stirred at −78° C. for 30 minutes. Methyl Iodide (48.2 g, 339.5 mmol) was added and stirring at −78° C. was continued for 4 hours. The reaction was quenched with saturated ammonium chloride solution, extracted into CH2Cl2 and washed with 1M sodium Bisulfite. The solution was dried over MgSO4, concentrated and chromatographed in 10% ethylacetate in hexane to give the titled compound (11.1 g, 56.5% yield) as an oil. MS, m/z (relative intensity): 1H NMR (400 MHz, CDCl3) δ ppm 0.8 (t, J=7.0 Hz, 3H) 0.9 (d, J=6.6 Hz, 3H) 1.0 (d, J=6.8 Hz, 3H) 1.0 (d, J=8.5 Hz, 1H) 1.1 (m, 1H) 1.4 (m, 1H) 1.7 (m, 1H) 3.7 (m, 1H) 4.2 (dd, J=8.8, 3.4 Hz, 1H) 4.6 (t, J=8.7 Hz, 1H) 5.4 (dd, J=8.7, 3.3 Hz, 1H) 7.2 (m, 2H) 7.3 (m, 3H). MS, m/z (relative intensity):290 [M+1H, 100%].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07388023B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-46f2404373214ce589a30c641b43fde6
출처 메모uspto-grants-2008_06