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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 501732생성일: 2026년 10월 24일

3-Hydroxybenzaldehyde → 3-Isopropoxybenzaldehyde

https://huagongshe.com/ko/reaction/501732

반응식

참여 물질

역할이름HCID투입량
반응물3-HydroxybenzaldehydeHCID 101—
반응물Isopropyl iodideHCID 6362—
반응물Potassium CarbonateHCID 11430—
반응물(S)-2,2,2-trifluoro-N-(6-methoxy-3-oxo-2,3-dihydro-1H-inden-1-yl)acetamideHCID 1472787—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물3-IsopropoxybenzaldehydeHCID 71291485%

반응 단계

Step AU (1). A solution of 3-hydroxybenzaldehyde (67 g, 549 mmol), 2-iodopropane (100 g, 588 mmol) and K2CO3 (130 g, 942 mmol) in 400 mL DMF was stirred for 18 h. To the above solution was added 2-iodopropane (20 g, 117 mmol) and K2CO3 (20 g, 145 mmol) and the mixture was stirred for another 24 h. The reaction mixture was poured into 300 mL water which was extracted with EtOAc (200 mL×3). The combined organic layers were washed with water (100 mL×3), dried over Na2SO4, filtered, and concentrated in vacuo to afford 77 g (85% yield) of 3-isopropoxybenzaldehyde as an oil. 1H NMR (300 MHz, CDCl3) δ 1.29-1.31 (d, 6H) 4.5-4.6 (m, 1H) 7.0-7.1 (m, 1H) 7.3-7.4 (m, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07772221B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-8571272274344ffcbf958067fbe99d83
출처 메모uspto-grants-2010_08