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HRID 56486作成日:2026年10月25日

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

https://huagongshe.com/reaction/56486

反応式

関与物質

役割名称HCID仕込み量
反応物BromoformHCID 5558—
反応物Potassium HydroxideHCID 14797—
反応物4-MorpholinobenzaldehydeHCID 291349—
反応物Potassium hydroxide methanolHCID 23689386—
溶媒MethanolHCID 887—
溶媒1,4-DioxaneHCID 31275—
生成物2-Methoxy-2-(4-morpholinophenyl)acetic acidHCID 5843210958%

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09434707B2
出典データセットuspto-grants-2016_09
ORD IDord-1e52a94da63c4f9db6dad8d67985954b
出典メモuspto-grants-2016_09