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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 854713생성일: 2026년 10월 24일

Methyl iodide → 1-o-Oleyl-2-o-methyl-3-o-trityl glycerol

https://huagongshe.com/ko/reaction/854713

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물Trityl chlorideHCID 6456—
반응물Sodium hydrideHCID 24758—
반응물Selachyl alcoholHCID 5282282—
용매WaterHCID 962—
용매PyridineHCID 1049—
용매TetrahydrofuranHCID 8028—
생성물1-o-Oleyl-2-o-methyl-3-o-trityl glycerolHCID 69470780—

반응 단계

Diol Compound 20 (2.0 g, 5.97 mmol) was added dropwise to a solution of trityl chloride (1.66 g, 6.0 mmol) in anhydrous pyridine (10 mL). The reaction was left to stir for 16 hours after which the solvent was removed by co-evaporation with toluene (2×5 mL). Then, part of the residue (1.0 g, 1.7 mol) was added dropwise to a suspension of NaH (0.14 g, 3.4 mmol) in THF (50 mL), followed by the addition of MeI (0.22 mL, 3.4 mmol). After 16 hours, TLC analysis showed that the reaction had gone to completion and H2O (5 mL) was added followed by concentration of the reaction mixture. The residue was partitioned between H2O (20 mL) and diethyl ether (100 mL), the organic extract was washed with sat NaHCO3 (10 mL), dried (MgSO4) and concentrated to give 1-O-oleyl-2-O-methyl-3-O-trityl glycerol (Compound 21) as an oil. Crude Compound 21 (1.16 g) was dissolved in CH2Cl2 (10 mL) after which trifluoroacetic acid (2 mL) was added. The reaction mixture was stirred for 5 min and excess TFA was quenched by adding solid NaHCO3 until effervescence ceased. The mixture was diluted with H2O (10 mL), extracted with CH2Cl2 (2×50 mL) and the combined organic phases were dried (MgSO4), concentrated and subjected to silica-gel column chromatography [eluent: hexane/ethyl acetate, 80/20, v/v] to give glycerol derivative Compound 22 (0.28 g, 42%) as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07259273B1
출처 데이터셋uspto-grants-2007_08
ORD IDord-b77d4f0319cc49ad9f0a3e71f3065e0d
출처 메모uspto-grants-2007_08