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HRID 459300作成日:2026年10月26日

1,2-Dibromoethane → (2S)-3-[4-(2-bromo-ethoxy)-phenyl]2-methoxy-propionic acid ethyl ester

https://huagongshe.com/reaction/459300

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-DibromoethaneHCID 7839—
反応物Potassium CarbonateHCID 11430—
反応物Sulfuric acid magnesium salt (1:1)HCID 24083—
反応物HCID 11390460HCID 11390460—
溶媒EthanolHCID 702—
生成物(2S)-3-[4-(2-bromo-ethoxy)-phenyl]2-methoxy-propionic acid ethyl esterHCID 58822865—

反応手順

A mixture containing (2S)-3-(4-hydroxy-phenyl)-2-methoxy-propionic acid ethyl ester obtained in Step 1 (0.223 mol, 50 mg), potassium carbonate (0.446 mol, 50 mg), magnesium sulfate (powdered, 50 mg, 1 g/g), ethylene dibromide (3.35 mol. 628 mg) and EtOH (25 mL) was heated at reflux (78–76° C.) for 24 hours and cool to room temperature. The mixture was heated again to reflux (76.5–77° C.) and 2 mL of ethylene dibromide was added. The mixture was heated for another 12 hours at 79.5–80.1° C. and then cooled to room temperature and vacuum filtered. The filtrate was concentrated under vacuum, and the residue was purified by column chromatography (silica gel, hexanes/ethyl acetate 6:1, Rf 027) to produce a colorless oil. MS (ES) for C14H19BrO4 [M+Na]+: 353.0.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07192982B2
出典データセットuspto-grants-2007_03
ORD IDord-9bdce17b3f9745cbabd0c9c4b53ffb28
出典メモuspto-grants-2007_03