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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 56486생성일: 2026년 10월 24일

Bromoform → 2-Methoxy-2-(4-morpholinophenyl)acetic acid

https://huagongshe.com/ko/reaction/56486

반응식

참여 물질

역할이름HCID투입량
반응물BromoformHCID 5558—
반응물Potassium HydroxideHCID 14797—
반응물4-MorpholinobenzaldehydeHCID 291349—
반응물Potassium hydroxide methanolHCID 23689386—
용매MethanolHCID 887—
용매1,4-DioxaneHCID 31275—
생성물2-Methoxy-2-(4-morpholinophenyl)acetic acidHCID 5843210958%

반응 단계

An oven-dried flask was charged with 4-(4-morpholinyl)benzaldehyde (10.1 g, 53 mmol), anhydrous methanol (60 mL) and anhydrous dioxane (60 mL) then fitted with an addition funnel. The addition funnel was charged with a solution of KOH (14.8 g, 264 mmol) in anhydrous methanol (60 mL) and an aliquot (˜2 mL) was added to the reaction mixture. Bromoform (5.8 mL, 67.1 mmol) was added to the reaction mixture then the remaining KOH/MeOH solution was added dropwise over 10 minutes. After stirring for 18 h, the mixture was filtered through Celite and rinsed with methanol. The filtrate was collected and concentrated in vacuo. The residue was then diluted with saturated aqueous NH4Cl and extracted with EtOAc. Additional EtOAc was then used to extract the aqueous phase while slowly adjusting the pH from ˜8 to ˜2 using concentrated HCl. A total of approximately 1.5 L of EtOAc was used for the extraction process. The combined EtOAc extracts were dried over Na2SO4 and filtered. Concentration of the filtrate in vacuo gave 2-methoxy-2-(4-morpholinophenyl)acetic acid as a tan solid (7.25 g, 58%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434707B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-1e52a94da63c4f9db6dad8d67985954b
출처 메모uspto-grants-2016_09