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HRID 508561作成日:2026年10月23日

2-Methyl-2-butene → 4-Amino-3-chloro-6-propyl-5-fluoropicolinic acid

https://huagongshe.com/ja/reaction/508561

反応式

関与物質

役割名称HCID仕込み量
反応物2-Methyl-2-buteneHCID 10553—
反応物Sodium Phosphate, DibasicHCID 24203—
反応物Sodium ChloriteHCID 23668197—
反応物4-Amino-3-chloro-5-fluoro-6-propylpicolinaldehydeHCID 86723400—
溶媒WaterHCID 962—
溶媒tert-ButanolHCID 6386—
生成物4-Amino-3-chloro-6-propyl-5-fluoropicolinic acidHCID 86723409—

反応条件

温度85 °C

反応手順

A microwave vial equipped with a magnetic stir bar was charged with 4-amino-3-chloro-6-propyl-5-fluoropicolinaldehyde (15.9 mg, 0.072 mmol) and t-butanol (1.0 mL). The mixture was treated with H2O (0.40 mL), 2-methylbut-2-ene (100 μL, 0.10 mmol), sodium hydrogenphosphate (21.6 mg, 0.100 mmol), and finally sodium chlorite (19.28 mg, 0.206 mmol) was added in one portion. The mixture was heated to 85° C. for 16 h. An aliquot of the reaction mixture was analyzed by LC-MS. LC-MS analysis showed one major product with the correct mass for the desired product. The reaction mixture was evaporated to dryness under N2. Purification via reverse phase chromatography yielded 4-amino-3-chloro-6-propyl-5-fluoropicolinic acid (4.7 mg, 27.9%): 1H NMR (400 MHz, CDCl3) δ 11.60 (s, 1H), 4.98 (m, 2H), 2.76 (m, 2H), 1.75 (m, 2H), 0.99 (m, 3H); 19F NMR (376 MHz, CDCl3) δ−139.98; ESIMS m/z 231.2 ([M−H]−).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09096526B2
出典データセットuspto-grants-2015_08
ORD IDord-f9257669cadb40fd971834e6b1dc1621
出典メモuspto-grants-2015_08