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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5593생성일: 2026년 10월 24일

Indole → 1-(4-Chlorobenzyl)-1h-indole

https://huagongshe.com/ko/reaction/5593

반응식

참여 물질

역할이름HCID투입량
반응물IndoleHCID 798—
반응물1-Chloro-4-(chloromethyl)benzeneHCID 7723—
반응물Potassium HydroxideHCID 14797—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물1-(4-Chlorobenzyl)-1h-indoleHCID 96716384.1%

반응 단계

A mixture of 11.72 g (0.1 mole) of indole, 17.71 g (0.11 mole) of 4-chlorobenzyl chloride, 33 g (0.5 mole) of 85% KOH, 14 mL of H2O, 2.5 g (2.5 mmoles) of PEG-1000 and 100 mL of toluene was stirred and heated at 55°-65° for 22 hours. After cooling to room temperature, 50 mL of H2O was added. The layers were separated. The aqueous layer was extracted with 100 mL of toluene. The combined organic phases were washed with 2N HCl (2×50 mL), H2O (2×50 mL), and 50 mL of brine and dried over MgSO4. Evaporation of the solvent left 29 g of orange-brown oil. The oil was chromatographed on a 1100 g column of silica gel. The column was eluted with 1:1 CH2Cl2 -Skellysolve B and 200 mL fractions were collected. The fractions were assayed by silica gel tlc (1×4") (25% CH2Cl2 -Skellysolve B). Fractions 12-19 were combined giving 23.11 g of crude product as a pink oil The oil was chromatographed on a 1100 g column of silica gel. The column was eluted with 25% CH2Cl2 -Skellysolve B and 200 mL fractions were collected. The fractions were assayed as before. Fractions 20-30 were combined giving 20.33 g (84%) of 1-(4-chlorobenzyl)indole as a yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05245046
출처 데이터셋uspto-grants-1993_09
ORD IDord-0aa88ee7cb854783bfc493ea25668c80
출처 메모uspto-grants-1993_09