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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 554542생성일: 2026년 10월 25일

Benzyl Bromide → 2-Benzyloxy-6-methoxybenzoic Acid Benzyl Ester

https://huagongshe.com/reaction/554542

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl BromideHCID 7498—
반응물Sodium hydrideHCID 24758—
반응물Ammonium ChlorideHCID 25517—
반응물2-Hydroxy-6-methoxybenzoic acidHCID 591524—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물2-Benzyloxy-6-methoxybenzoic Acid Benzyl EsterHCID 67461231118.8%

반응 단계

While stirring a mixture of 6-methoxysalicylic acid (5.07 g, 30.15 mmol) and sodium hydride (60% w/w, 3.02 g, 75.38 mmol) under cooling with ice, DMF (30 mL) was added thereto. The mixture solution was stirred at the same temperature for 10 minutes, and then benzyl bromide (8.95 mL, 75.38 mmol) was added thereto over 5 minutes and the reaction mixture was stirred at the same temperature for 30 minutes and at room temperature for 2.5 hours. To the reaction mixture was added a saturated ammonium chloride aqueous solution and water under cooling with ice, and the mixture was extracted with ether. The organic layer was washed with water and a saturated ammonium chloride aqueous solution and dried (anhydrous sodium sulfate), and then the solvent was distilled under reduce pressure. The obtained residue was purified by silica gel column chromatography [developing solution=ethyl acetate:n-hexane (1:10 to 1:5)] to obtain the title compound (6.24 g, 59%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08048897B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-b529aa7dabe94287b9e915ab20f82d76
출처 메모uspto-grants-2011_11