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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 19834생성일: 2026년 10월 24일

Acetone → 4-(beta-D-glucopyranos-1-yl)-2-(4-trifluoromethoxy-benzyl)-benzonitrile

https://huagongshe.com/ko/reaction/19834

반응식

참여 물질

역할이름HCID투입량
반응물AcetoneHCID 180—
반응물Potassium CarbonateHCID 11430—
반응물4-(Trifluoromethoxy)phenylboronic acidHCID 2734386—
반응물2-Bromomethyl-4-(2,3,4,6-tetra-O-acetyl-D-glucopyranos-1-yl)-benzonitrileHCID 67131410—
촉매Palladium ChlorideHCID 24290—
용매WaterHCID 962—
용매Sodium chloride; waterHCID 57417360—
생성물4-(beta-D-glucopyranos-1-yl)-2-(4-trifluoromethoxy-benzyl)-benzonitrileHCID 86618956—

반응 단계

An Ar filled flask is charged with 2-bromomethyl-4-(2,3,4,6-tetra-O-acetyl-D-glucopyranos-1-yl)-benzonitrile (0.25 g), 4-trifluoromethoxy-phenylboronic acid (0.20 g), potassium carbonate (0.26) and a 3:1 mixture of degassed acetone and water (4 mL). The mixture is stirred at room temperature for 5 min, before it is cooled in an ice-bath. Then palladium dichloride (5 mg) is added and the reaction mixture is stirred for 16 h at ambient temperature. The mixture is then diluted with brine and extracted with ethyl acetate. The combined extracts are dried over sodium sulfate and the solvent is removed under reduced pressure. The residue is dissolved in methanol (9 mL) and treated with 4 M aqueous potassium hydroxide solution (1 mL). The resulting solution is stirred at ambient temperature for 1 h and then neutralized with 1 M hydrochloric acid. The methanol is evaporated, and the residue is diluted with brine and extracted with ethyl acetate. The organic extracts collected are dried over sodium sulfate, and the solvent is removed. The residue is chromatographed on silica gel (dichloromethane/methanol 1:0->8:1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745414B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-2978893eff4643ecbe663c6f7d435a8a
출처 메모uspto-grants-2010_06