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HRID 35921생성일: 2026년 10월 23일

Trimethylsilylacetylene → 4-[4-Trimethylsilyl-(1,2,3-triazol-1-yl) methyl]benzonitrile

https://huagongshe.com/ko/reaction/35921

반응식

참여 물질

역할이름HCID투입량
반응물TrimethylsilylacetyleneHCID 66111—
반응물4-(Azidomethyl)benzonitrileHCID 11073691—
용매TolueneHCID 1140—
생성물4-[4-Trimethylsilyl-(1,2,3-triazol-1-yl) methyl]benzonitrileHCID 19104242—

반응 단계

38.9 g of 4-azidomethylbenzonitrile is refluxed in 400 ml of toluene with 42 ml of trimethylsilylacetylene for 5 hours at 120° , combined with another 21 ml of trimethylsilylacetylene, and once again refluxed for 3 hours at 1.20° Then the mixture is concentrated under vacuum, yielding 63 g of crude 4-[4-trimethylsilyl-(1,2,3-triazol-1-yl) methyl]benzonitrile. The latter is refluxed with a mixture of 700 ml of glacial acetic acid, 380 ml of water, as well as 110 ml of tetrahydrofuran for 2 hours. For working up purposes, the mixture is poured into sodium bicarbonate solution, extracted three times with dichloromethane, washed neutral with water, dried over sodium sulfate, concentrated to dryness under vacuum, and recrystallized from ethyl acetate/hexane yielding 32 8 g of 4-[1-(1,2,3-triazolyl)methyl]benzonitrile as colorless crystals, mp 83°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05411982
출처 데이터셋uspto-grants-1995_05
ORD IDord-f0035496a7e54c9f94767f9f6a0c8d04
출처 메모uspto-grants-1995_05