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HRID 885501作成日:2026年10月26日

Hydrochloric Acid → (R)-2-(4-Fluoro-3,5-dimethyl-phenylamino)-hexanoic acid

https://huagongshe.com/reaction/885501

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Potassium CarbonateHCID 11430—
反応物Norleucine, D-(-)-HCID 456468—
反応物5-Bromo-2-fluoro-1,3-dimethylbenzeneHCID 2736298—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
溶媒DimethylacetamideHCID 31374—
生成物(R)-2-(4-Fluoro-3,5-dimethyl-phenylamino)-hexanoic acidHCID 69189506—

反応条件

温度90 °C

反応手順

(R)-2-Amino-hexanoic acid (0.840 g, 6.4 mmol), 5-bromo-2-fluoro-1,3-dimethyl-benzene (1.292 g, 6.4 mmol), CuI (0.122 g, 0.64 mmol), and K2CO3 (1.326 g, 9.6 mmol) were weighed into a Schlenk flask. To this was added 8 mL of dimethylacetamide and the resulting mixture vacuum-pumped and nitrogen-filled alternatively three times. After heating to 90° C. with stirring for 39 h, the reaction mixture was cooled to room temperature, diluted with 20 mL of ethyl acetate and 10 mL of water, and then acidified with concentrated HCl to pH=3. The layers were separated and the aqueous layer extracted with ethyl acetate (20 mL×5). The organic layers were combined and dried over anhydrous Na2SO4. Removal of the solvent under reduced pressure gave the title product which was used directly in the next step with further purification. LC-MS: tR=8.5 min, m/z 254 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08242174B2
出典データセットuspto-grants-2012_08
ORD IDord-fa77dd1252564d68b6b8a2dd1d36679e
出典メモuspto-grants-2012_08