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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 277736생성일: 2026년 10월 26일

Benzyl azide → 1-Phenylmethyl-4-(2,4,6-trimethylphenyl)-5-aminotriazole

https://huagongshe.com/reaction/277736

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl azideHCID 12152—
반응물2,4,6-TrimethylphenylacetonitrileHCID 520698—
반응물Potassium tert-butoxideHCID 23665647—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물1-Phenylmethyl-4-(2,4,6-trimethylphenyl)-5-aminotriazoleHCID 1548698261%

반응 단계

A mixture of 2,4,6-trimethylbenzyl cyanide (1.0 g, 6.3 mmol), benzyl azide (0.92 g, 6.9 mmol) and potassium t-butoxide (0.78 g, 6.9 mmol) in tetrahydrofuran (10 mL) was stirred at ambient temperature for 2.5 days. The resulting suspension was diluted with water and extracted three times with ethyl acetate. The combined organic layers were dried over MgSO4 and filtered. Solvent was removed in vacuo to give a brown oil. Trituration with ether and filtration afforded a yellow solid (1.12 g, 61% yield): NMR (CDCl3, 300 MHz):7.60-7.30 (m, 5H), 7.30-7.20 (m, 2H), 5.50 (s, 2H), 3.18 (br s, 2H), 2.30 (s, 3H), 2.10 (s, 6H); CI-MS: 293 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06358950B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-ab652eea6daa4c4ea43e3f4aa3c4d422
출처 메모uspto-grants-2002_03