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HRID 50731作成日:2026年10月26日

p-Toluenesulfonic acid → Methyl 3-bromo-2-fluorobenzoate

https://huagongshe.com/reaction/50731

反応式

関与物質

役割名称HCID仕込み量
反応物p-Toluenesulfonic acidHCID 6101—
反応物Trimethyl orthoformateHCID 9005—
反応物3-Bromo-2-fluorobenzoic acidHCID 2736313—
溶媒MethanolHCID 887—
生成物Methyl 3-bromo-2-fluorobenzoateHCID 2158450584%

反応手順

A solution of 3-bromo-2-fluorobenzoic acid (0.219 g, 1 mmol) in dry methanol (5 mL) under nitrogen was treated with trimethylorthoformate (0.22 mL, 2 mmol) and p-toluenesulfonic acid (catalytic amount), and then heated under reflux. After 16 h, the mixture was evaporated and the residue partitioned between water and Et2O. The organic layer was washed with sat. sodium hydrogen carbonate solution, water, brine, dried (MgSO4) and evaporated to give methyl 3-bromo-2-fluorobenzoate (0.195 g, 0.84 mmol, 84%): 1H-NMR (CDCl3) δ 7.90-7.85 (m, 1H), 7.71-7.65 (m, 1H), 7.10 (dt, 1H, J=8.0, 1.0 Hz), 3.94 (s, 3H): MS (EI) 232 (M+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06713478B2
出典データセットuspto-grants-2004_03
ORD IDord-98d25844ab9a45b0be12bcafe456a4ba
出典メモuspto-grants-2004_03