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HRID 6905作成日:2026年10月23日

Hydrochloric Acid → 3-Fluoro-4-methylanisole

https://huagongshe.com/ja/reaction/6905

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Tetrafluoroboric acidHCID 28118—
反応物5-Methoxy-o-toluidineHCID 99500—
反応物Sodium NitriteHCID 23668193—
溶媒WaterHCID 962—
生成物3-Fluoro-4-methylanisoleHCID 277457131%

反応条件

温度0 °C

反応手順

A mixture of 5-methoxy-2-methyl aniline (5.0 g; 36 mmol), HCl (7.6 mL of a 12 M solution; 91 mmol) and H2O (11 mL) was heated at 60° C. for 15 min until complete dissolution had occurred. The reaction was cooled to 0° C. and an aqueous solution of NaNO2 (2.5 g; 36 mmol) was added dropwise (internal temperature ≦7° C.). The reaction was stirred at 0° C. for 30 min and a 0° C. solution of HBF4 (5.3 mL of a 48% solution; 40 mmol) was added cautiously. The reaction was stirred at 0° C. for 20 min, and the resultant brown solid was filtered, washed with ice water (3×10 mL) and H2O (2×10 mL). The solid was dried under high vacuum for 20 h, then heated (heat gun) until evolution of BF3 (white fumes) had ceased. The resulting brown oil was partitioned between EtOAc and H2O. The organic phase was dried (Na2SO4), concentrated in vacuo and distilled by Kugelrohr to give 3-fluoro-4-methyl anisole (1.6 g; 31%) as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07084162B2
出典データセットuspto-grants-2006_08
ORD IDord-0b4e7c8c64764d9385bb00888530814d
出典メモuspto-grants-2006_08