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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2061784생성일: 2026년 10월 26일

Chloroform → 9-Allylcarbazole

https://huagongshe.com/reaction/2061784

반응식

참여 물질

역할이름HCID투입량
반응물ChloroformHCID 6212—
반응물CarbazoleHCID 6854—
반응물Allyl bromideHCID 7841—
반응물Potassium HydroxideHCID 14797—
용매Dimethyl SulfoxideHCID 679—
생성물9-AllylcarbazoleHCID 3090393100%

반응 단계

Carbazole (10.1 g, 0.057 mol) and potassium hydroxide (88% wt pellets, crushed, 7.1 g, 0.11 mol) were stirred in 100 mL DMSO at 50° C. for 30 min before dropwise addition of allyl bromide (14.7 g, 0.118 mol). After 15 min the reaction mixture was poured into a 500 mL separatory funnel containing 100 mL chloroform and washed 5 times with 200 mL water to give, after solvent evaporation at 60° C. under reduced pressure, compound 15 in >99% purity as a dark brown, viscous syrup which solidified upon cooling (11.9 g, 0.057 mol, 100% yield). 1H NMR (300 MHz, CDCl3): δ=8.14-8.06 (m, 2 carbazole H), 7.49-7.32 (m, 4 carbazole H), 7.28-7.19 (m, 2 carbazole H), 6.04-5.90 (m, CH═CH2), 5.19-5.10 (m, Z-HCH═CH), 5.07-4.97 (m, E-HCH═CH), 4.92-4.85 (m, NCH2). 13C NMR (300 MHz, CDCl3): δ=140.34, 132.27, 125.67, 122.90, 120.33, 119.00, 116.74, 108.74, 45.21.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08283438B2
출처 데이터셋uspto-grants-2012_10
ORD IDord-6bb917780b754dc9afb9efe31616f4bc
출처 메모uspto-grants-2012_10