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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 636830생성일: 2026년 10월 25일

Toluene → HCID 54505552, 화합물

https://huagongshe.com/reaction/636830

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물4-Fluorobenzyl bromideHCID 68021—
반응물Potassium bis(trimethylsilyl)amideHCID 3251421—
반응물1-Benzyl 4-tert-butyl 2-methyl piperazine-1,2,4-tricarboxylateHCID 4451965—
용매DimethylformamideHCID 6228—
용매TetrahydrofuranHCID 8028—
생성물HCID 54505552HCID 54505552—

반응 조건

온도-78 °C

반응 단계

To a stirred solution of piperazine-1,2,4-tricarboxylic acid 1-benzyl ester 4-tert-butyl ester 2-methyl ester (10.5 g, 27.8 mmol), prepared as described by Bigge et al. (Tetrahedron Let. 1989, 30, 5193), in tetrahydrofuran (200 mL) under a nitrogen atmosphere was added N,N-dimethylformamide (30 mL). The reaction was cooled to about −78° C., and a 0.5 M solution of potassium bis(trimethylsilyl)amide in toluene (83 mL, 42 mmol) was added. The reaction was stirred at about −78° C. for about 1 hour, and then 4-fluorobenzyl bromide (5.2 mL, 42 mmol) was added. The reaction was stirred for about 1 hour more at about −78° C., then warmed to room temperature and stirred overnight. The reaction was quenched with saturated sodium bicarbonate solution, and the mixture was extracted three times with ethyl acetate. The combined organic layers were extracted twice with water, brine, dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo to give the crude product as a yellow oil. Purification by silica gel chromatography using 0-20% ethyl acetate/hexanes as eluent afforded the title compound of part 1-A (8.54 g, 63%) as a colorless oil: +APcI MS (M−Boc+H)+ 387; 1H NMR=400 MHz (CDCL3) δ: 7.45-7.30 (arom, br s, 5H), 7.00-6.80 (arom, br m, 4H), 5.35-5.05 (br m, 2H), 2.53 (br t, 1H), 1.40 (Boc, s, 9H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06194578B1
출처 데이터셋uspto-grants-2001_02
ORD IDord-5e588bb12b574a7abf3ae99bcbf219f4
출처 메모uspto-grants-2001_02