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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 48071생성일: 2026년 10월 24일

3-Hydroxybenzaldehyde → 3-Tert-butoxybenzaldehyde

https://huagongshe.com/ko/reaction/48071

반응식

참여 물질

역할이름HCID투입량
반응물3-HydroxybenzaldehydeHCID 101—
반응물Boron trifluoride etherateHCID 8000—
반응물Sodium BicarbonateHCID 516892—
반응물Tert-butyl 2,2,2-trichloroethanimidateHCID 2734700—
용매DichloromethaneHCID 6344—
용매HexaneHCID 8058—
용매CyclohexaneHCID 8078—
용매Ethyl AcetateHCID 8857—
생성물3-Tert-butoxybenzaldehydeHCID 1571222432%

반응 단계

Ex-654A) 3-Hydroxybenzaldehyde (4.08 g, 33.4 mmol) was slurried in 50 mL of anhydrous CH2Cl2 and added to t-butyl-2,2,2-trichloroacetimidate (25.0 g, 114 mmol) in 200 mL of anhydrous cyclohexane with an additional 50 mL of CH2Cl2 used in transfer. The mixture was stirred under nitrogen until uniform, then boron trifluoride diethyl etherate (0.50 μL, 4 mmol) was added via syringe and stirring was continued for 1 h. Powdered sodium bicarbonate (50 g, 0.6 mol) was added, and the solution was filtered through a silica gel plug, washing the plug with hexane. The solvent was evaporated to give crude product 3.54 g (59%) as an amber oil (85% pure by GC analysis). Chromatography on silica gel eluting with 0-10% ethyl acetate in hexane gave 1.88 g (32%) of pure 3-t-butoxybenzaldehyde product as a colorless oil. 1H NMR (C6D6) δ9.59 (s, 1H), 7.44 (br s, 1H), 7.20 (d t, 1H), 6.92 (m, 2H), 1.07 (s, 9H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06699898B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-c11ac5ee86c947019e21107d646b7ad3
출처 메모uspto-grants-2004_03