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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 56503생성일: 2026년 10월 23일

Bromoform → 2-(4-Isopropoxyphenyl)-2-methoxyacetic acid

https://huagongshe.com/ko/reaction/56503

반응식

참여 물질

역할이름HCID투입량
반응물BromoformHCID 5558—
반응물Potassium HydroxideHCID 14797—
반응물1,4-DioxaneHCID 31275—
반응물4-IsopropoxybenzaldehydeHCID 250077—
반응물Potassium hydroxide methanolHCID 23689386—
용매MethanolHCID 887—
생성물2-(4-Isopropoxyphenyl)-2-methoxyacetic acidHCID 58432042—

반응 단계

An oven-dried flask was charged with 4-isopropoxybenzaldehyde (4.9 g, 29.9 mmol), anhydrous methanol (30 mL) and anhydrous dioxane (30 mL) then fitted with an addition funnel. The addition funnel was charged with a solution of KOH (8.4 g, 149.5 mmol) in anhydrous methanol (30 mL) and an aliquot (˜2 mL) was added to the reaction mixture. Bromoform (3.4 mL, 38.8 mmol) was added to the reaction mixture then the remaining KOH/MeOH solution was added dropwise over 10 minutes. After stirring for 18 hours, the mixture was concentrated in vacuo. The residue was diluted with water and the pH was adjusted to ˜2 using concentrated HCl then extracted with EtOAc. The combined organics were dried over Na2SO4 and filtered. Concentration of the filtrate in vacuo gave 2-(4-isopropoxyphenyl)-2-methoxyacetic acid as a light yellow solid (6.8 g) which was used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434707B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-e9c5eccb47884e1e8730c24ca8b655c2
출처 메모uspto-grants-2016_09