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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 9102생성일: 2026년 10월 23일

Benzonitrile → 2-Aminobenzothiazole-6-carbonitrile

https://huagongshe.com/ko/reaction/9102

반응식

참여 물질

역할이름HCID투입량
반응물BenzonitrileHCID 7505—
반응물4-AminobenzonitrileHCID 13396—
반응물BromineHCID 24408—
반응물Potassium thiocyanateHCID 516872—
용매Acetic AcidHCID 176—
용매WaterHCID 962—
생성물2-Aminobenzothiazole-6-carbonitrileHCID 432713967.4%

반응 조건

온도16 °C

반응 단계

Two grams of 4-aminobenzonitrile was dissolved in about 40 mL acetic acid and the solution was cooled to about 16° C. About 3.3 g of potassium thiocyanate was added and the flask was equipped with an addition funnel. The addition funnel was charged with about 2.7 g bromine and about 5 mL acetic acid. This dark solution was then added to the benzonitrile solution in a dropwise fashion under good agitation and allowed to stir for about 16 hours. The slurry was then drowned into water and filtered. The presscake was washed well with water, reslurried in dilute aqueous alkali and filtered. Again the presscake was washed well with water. After drying in vacuo, about 2 grams of the title compound was isolated. 1H NMR 6.8 (d, 1H, J=8.7 Hz), 6.9 (br s, 2H), 7.6 (dd, 1H, J=2 Hz, J=8.7 Hz), 8.0 (d, 1H, J=2 Hz), LC/MS 2.34 min, 174 (M−H−), RP-HPLC RT 7.7 minutes.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091227B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-5037c9c33a5a49e9b0b5c20797e25f9c
출처 메모uspto-grants-2006_08