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HRID 1874생성일: 2026년 10월 23일

Hydrogen Peroxide → 4-t-Butoxy-2,3,6-trifluoro-5-hydroxypyridine

https://huagongshe.com/ko/reaction/1874

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen PeroxideHCID 784—
반응물Trimethyl borateHCID 8470—
반응물Sodium HydroxideHCID 14798—
반응물Lithium diisopropylamideHCID 2724682—
반응물4-t-Butoxy-2,3,6-trifluoropyridineHCID 10608547—
용매Acetic AcidHCID 176—
용매TetrahydrofuranHCID 8028—
생성물4-t-Butoxy-2,3,6-trifluoro-5-hydroxypyridineHCID 10656587—

반응 조건

온도-78 °C

반응 단계

A 11.16 g (54.39 mmol) sample of 4-t-butoxy-2,3,6-trifluoropyridine, from Example 253 step b above, was dissolved in 50 mL of THF, and the solution was cooled to -78° C. To this solution was added LDA (65.6 mmol) with stirring for 30 min, during which a solid preciptated. To this mixture was added 7.5 mL of trimethoxyborane, with stirring for 25 min at -78° C. To this mixture was added 10 mL of acetic acid, and the mixture was stirred and allowed to warm to room temperature. Next was added 100 mL of 30% hydrogen peroxide and 100 mL of 2N sodium hydroxide while cooling in an ice bath. The mixture was then stirred at room temperature for 16 hours, and quenched with saturated NH4Cl solution. The mixture was extracted with ether, and the extract was washed with brine and dried over MgSO4. The solvent was removed under vacuum, and the residue was purified by flash chromatography on silica gel, eluting with 1:8 ethyl acetate:hexane. Removal of the solvent gave 9.769 g of the title product as a colorless liquid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05726182
출처 데이터셋uspto-grants-1998_03
ORD IDord-c191750ca7b54fdb8dafaf0853defb9d
출처 메모uspto-grants-1998_03