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HRID 55378作成日:2026年10月25日

Acetyl chloride → Methyl 3-fluoro-4-nitrobenzoate

https://huagongshe.com/reaction/55378

反応式

関与物質

役割名称HCID仕込み量
反応物Acetyl chlorideHCID 6367—
反応物3-Fluoro-4-nitrobenzoic acidHCID 230653—
溶媒MethanolHCID 887—
生成物Methyl 3-fluoro-4-nitrobenzoateHCID 592761—

反応手順

To a solution prepared by the dropwise addition of 12 ml acetyl chloride to 150 ml methanol was added 7.0 grams 3-fluoro-4-nitrobenzoic acid and the resulting mixture was stirred at room temperature for 18 hours. The solvent was removed in vacuo and the residue was partitioned between ethyl acetate and 2% sodium carbonate solution. The organic layer was washed with saturated sodium chloride solution, dried over magnesium sulfate, filtered, and evaporated in vacuo to give 6 grams of methyl 3-fluoro-4-nitrobenzoate as an orange oil which gradually hardened to a yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05624957
出典データセットuspto-grants-1997_04
ORD IDord-05ac5c8e382847e08303bf53883c12df
出典メモuspto-grants-1997_04