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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 54871생성일: 2026년 10월 23일

1-Iodooctane → (5R)-3-(4-octyloxyphenyl)-5-phenyl-2-oxazolidinone

https://huagongshe.com/ko/reaction/54871

반응식

참여 물질

역할이름HCID투입량
반응물1-IodooctaneHCID 12380—
반응물Sodium hydrideHCID 24758—
반응물(5R)-3-(4-hydroxyphenyl)-5-phenyl-2-oxazolidinoneHCID 54314065—
용매DimethylformamideHCID 6228—
생성물(5R)-3-(4-octyloxyphenyl)-5-phenyl-2-oxazolidinoneHCID 5363792930.1%

반응 단계

Then, 0.30 g (1.18 mM) of (5R)-3-(4-hydroxyphenyl)-5-phenyl-2-oxazolidinone and 4.6 ml of DMF were placed in 30 ml-round bottomed flask, followed by stirring to form a solution. To the solution, 0.053 g (1.33 mM) of 60%-oily sodium hydride was added under stirring at room temperature. After the settlement of foaming, 0.25 ml (1.38 mM) of 1-iodooctane was added to the mixture, followed by stirring for 30 minutes on an oil bath kept at about 70° C. After the reaction, the reaction mixture was poured into ice water to precipitate a crystal. The crystal was recovered by filtration and washed with water, followed by purification by silica gel column chromatography (eluent: toluene/ethyl acetate =100/1) and recrystallization from a toluene-methanol mixture solvent to obtain 0.13 g of (5R)-3-(4-octyloxyphenyl)-5-phenyl-2-oxazolidinone (Yield: 30.1%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05624600
출처 데이터셋uspto-grants-1997_04
ORD IDord-ccc751841a9b4b238bdcd8e8f959367b
출처 메모uspto-grants-1997_04