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HRID 41178作成日:2026年10月26日

Hydrochloric Acid → Methyl 3-bromo-4-hydroxy-5-(3-morpholino-3-oxopropanoyl)benzoate

https://huagongshe.com/reaction/41178

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物4-Morpholinecarbonyl chlorideHCID 84810—
反応物Lithium HexamethyldisilazideHCID 2733832—
反応物Methyl 3-acetyl-5-bromo-4-hydroxybenzoateHCID 15818980—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl 3-bromo-4-hydroxy-5-(3-morpholino-3-oxopropanoyl)benzoateHCID 5823504090.2%

反応条件

温度0 °C

反応手順

To a solution of lithium bis(trimethylsilyl)amide (1.41 L, 1406 mmol) at −65° C. under nitrogen was added dropwise methyl 3-acetyl-5-bromo-4-hydroxybenzoate (120 g, 439 mmol) in THF (1.2 L). The solution was allowed to warm to 0° C., and maintained at this temperature for 1 h. The solution was cooled back to −65° C. and morpholine-4-carbonyl chloride (0.055 L, 483 mmol) was added. The mixture was stirred at room temperature for 2 h then cooled to −30° C., DCM (1.5 L) and water (1 L) were added followed by dropwise addition of HCl 6N (500 mL) then HCl 2N (300 mL) until pH 7, the aqueous solution was extracted with DCM (3×). The combined extracts were dried over MgSO4 and evaporated. The crude product was triturated in MTBE to obtain methyl 3-bromo-4-hydroxy-5-(3-morpholino-3-oxopropanoyl)benzoate (153 g, 90%) as a beige solid. Mass Spectrum: m/z [M+H]+=388.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08530470B2
出典データセットuspto-grants-2013_09
ORD IDord-ac98ea7eac74444ebae29bd7fb48f7ea
出典メモuspto-grants-2013_09