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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 6905생성일: 2026년 10월 23일

Hydrochloric Acid → 3-Fluoro-4-methylanisole

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

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Tetrafluoroboric acidHCID 28118—
반응물5-Methoxy-o-toluidineHCID 99500—
반응물Sodium NitriteHCID 23668193—
용매WaterHCID 962—
생성물3-Fluoro-4-methylanisoleHCID 277457131%

반응 조건

온도0 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07084162B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-0b4e7c8c64764d9385bb00888530814d
출처 메모uspto-grants-2006_08