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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 964015생성일: 2026년 10월 25일

Borane → 6-(2-hydroxyethyl)-3-methyloxazolo[4,5-b]pyridin-2(3H)-one

https://huagongshe.com/reaction/964015

반응식

참여 물질

역할이름HCID투입량
반응물BoraneHCID 6331—
반응물2,3-Dimethyl-1-buteneHCID 11249—
반응물Sodium HydroxideHCID 14798—
반응물InChI=1/C6H15B/c1-5(2)6(3,4)7/h5H,7H2,1-4HHCID 5326179—
반응물3-methyl-6-vinyloxazolo[4,5-b]pyridin-2(3H)-oneHCID 19079286—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물6-(2-hydroxyethyl)-3-methyloxazolo[4,5-b]pyridin-2(3H)-oneHCID 1907931778%

반응 조건

온도0 °C

반응 단계

A solution of boron hydride (1M in tetrahydrofuran) (5 ml, 5 mmol) is cooled using a salt/ice bath, and then 2,3-dimethyl-1-butene (0.6 ml, 5 mmol) are slowly added. The temperature of the solution is increased to 0° C. and stirring is maintained for a further 2 hours at that temperature. 3-methyl-6-vinyloxazolo[4,5-b]pyridin-2(3H)-one (1.14 mg, 5 mmol) dissolved in tetrahydrofuran (20 ml) is added to the previously prepared solution of thexylborane. The whole is stirred at 0° C. for 2 hours, then a 10% aqueous sodium hydroxide solution (2.40 ml) and also oxygenated water (2.00 ml) are added in succession. After 1 hour's stirring at room temperature and evaporation of the solvent under reduced pressure, the residue is taken up in water. Extraction is carried out with dichloromethane; the organic phase is dried over magnesium sulfate and filtered, and then the solvent is evaporated off under reduced pressure. Purification by flash chromatography on silica gel (eluant: dichloromethane/methanol: 95/5) yields 6-(2-hydroxyethyl)-3-methyloxazolo[4,5-b]pyridin-2(3H)-one in a yield of 78%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05767128
출처 데이터셋uspto-grants-1998_06
ORD IDord-39ea5d17b9744646b760e50c6526fb59
출처 메모uspto-grants-1998_06