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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1068579생성일: 2026년 10월 26일

Hydrochloric Acid → 3,4-Dimethoxyphenyl 2-thiazolyl ketone

https://huagongshe.com/reaction/1068579

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물3,4-DimethoxybenzonitrileHCID 74842—
반응물2-BromothiazoleHCID 76430—
반응물Sodium BicarbonateHCID 516892—
반응물ButyllithiumHCID 178418339—
용매Diethyl EtherHCID 3283—
용매HexaneHCID 8058—
생성물3,4-Dimethoxyphenyl 2-thiazolyl ketoneHCID 2118976846.5%

반응 조건

온도-78 °C

반응 단계

A hexane solution of butyllithium (9.50 mM) was dissolved in dried diethyl ether (6.5 ml) and cooled to −78° C. A solution of 2-bromothiazole (1.03 g, 6.13 mM) in diethyl ether (0.5 ml) was dropped into this solution. The solution was stirred at that temperature for 30 minutes, then a solution of 3,4-dimethoxybenzonitrile (1.00 g, 6.13 mM) in diethyl ether (3.0 ml) was added and the resultant mixture stirred for a further 6 hours. 1N Hydrochloric acid (20 ml) was poured into the solution obtained, which was then warmed to room temperature and stirred for 30 minutes, then a saturated sodium hydrogencarbonate solution was added to neutralize the solution and extraction was performed with ethyl acetate. Next, the organic layer was washed with brine and dried over anhydrous magnesium sulfate, then the solvent was removed in vacuo to obtain a dark red solid residue. The residue was purified by flash chromatography (SiO2: eluted by gradient from 50% hexane/methylene chloride to 25% hexane/methylene chloride). The solvent was removed in vacuo and the resultant product was dried to obtain 3,4-dimethoxyphenyl 2-thiazolyl ketone 0.71 g (yield 46.5%) as a red solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06251897B1
출처 데이터셋uspto-grants-2001_06
ORD IDord-39e331ceaef847f59d5e01b8cee33013
출처 메모uspto-grants-2001_06