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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 13764생성일: 2026년 10월 23일

Ammonium Chloride → 4-(1-Methylpiperidin-4-yloxy)-3-trifluoromethylbenzonitrile

https://huagongshe.com/ko/reaction/13764

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물4-Piperidinol, 1-methyl-HCID 66048—
반응물4-Fluoro-3-(trifluoromethyl)benzonitrileHCID 144255—
반응물Potassium tert-butoxideHCID 23665647—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물4-(1-Methylpiperidin-4-yloxy)-3-trifluoromethylbenzonitrileHCID 2314594064.8%

반응 단계

6.68 g of potassium t-butoxide was suspended in 40 ml of anhydrous tetrahydrofuran and a solution of 6.85 g of 1-methyl-4-hydroxypiperidine in 20 ml of anhydrous tetrahydrofuran was added dropwise over 35 minutes while stirring under ice-water cooling and further the mixture was stirred for 30 minutes. On the other hand, 7.50 g of 4-fluoro-3-trifluoromethylbenzonitrile was dissolved in 40 ml of anhydrous tetrahydrofuran, the mixture was stirred under cooling in a dry ice/acetone bath, and the solution prepared earlier was added dropwise at the internal temperature of −70° C. After adding dropwise, the reaction solution was stirred overnight while naturally heating up to room temperature. The reaction solution was ice-cooled, an aqueous saturated ammonium chloride solution and water were added thereto, and then the solvent was distilled off under reduced pressure. The residue was subjected to extraction with ethyl acetate twice. The extracts were washed in turn with water and saturated saline and dried over anhydrous magnesium sulfate, and then the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography to obtain 7.31 g of the objective compound as colorless crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728131B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-ac5ac920425a4ccd89ccd021d933c772
출처 메모uspto-grants-2010_06