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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1463549생성일: 2026년 10월 25일

P-Anisidine → 4-Methoxybenzenediazonium tetrafluoroborate

https://huagongshe.com/reaction/1463549

반응식

참여 물질

역할이름HCID투입량
반응물P-AnisidineHCID 7732—
반응물Nitrous AcidHCID 24529—
반응물Tetrafluoroboric acidHCID 28118—
반응물Sodium NitriteHCID 23668193—
용매WaterHCID 962—
생성물4-Methoxybenzenediazonium tetrafluoroborateHCID 517233—

반응 단계

p-Anisidine (30.75 g, 0.25 mole) was dissolved in aqueous tetrafluoroboric acid (48%, 110 ml) in a 500 ml 3 necked flask fitted with mechanical stirring, and cooled to 0°-10° C. Sodium nitrite (17.5 g, 0.25 mole) was separately dissolved in water (34 ml) and the solution cooled to 5°-10° C., and was then added dropwise to the reaction mixture over 60 minutes. The reaction mixture was stirred for about 45 minutes at 0°-10° C., and then tested with starch-iodide paper for excess nitrous acid. Any excess nitrous acid was destroyed by adding a small amount (approx. 0.1 g.) of sulfamic acid. The precipitate was filtered, washed once with ice-cold water (about 30 ml), and then twice with methanol (20 ml each time). The product diazonium tetrafluoroborate was dried under vacuum at ambient temperature. Yield 45.4 g (about 82%). This could be purified by dissolving in minimum amount of acetone, and precipitating with ether, repeating this process three times. The final product was filtered, washed with ether (30 ml), and dried.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05300675
출처 데이터셋uspto-grants-1994_04
ORD IDord-975f9b7fd5454c5da3433d567ba07d9e
출처 메모uspto-grants-1994_04