Hydrochloric Acid → 3-Fluoro-4-methylanisole

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.

1. addition40 mmol) was added cautiously
2. filtrationthe resultant brown solid was filtered
3. washwashed with ice water (3×10 mL) and H2O (2×10 mL)
4. customThe solid was dried under high vacuum for 20 h
5. temperatureheated
6. temperature(heat gun) until evolution of BF3 (white fumes)
7. customThe resulting brown oil was partitioned between EtOAc and H2O
8. dry with materialThe organic phase was dried (Na2SO4)
9. concentrationconcentrated in vacuo
10. distillationdistilled by Kugelrohr

ORDレコード

ord-0b4e7c8c64764d9385bb00888530814d

出典データセット

uspto-grants-2006_08

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US07084162B2