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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2188382생성일: 2026년 10월 25일

Ammonium Chloride → 2-[(3,4-Dichlorophenyl)dimethylaminomethyl]-1-phenethylcyclo-hexanol, hydrochloride

https://huagongshe.com/reaction/2188382

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물2-[(3,4-Dichlorophenyl)dimethylaminomethyl]cyclohexanoneHCID 69942917—
반응물Chlorotrimethylsilane waterHCID 86753056—
반응물HCID 178418865HCID 178418865—
용매Methyl Ethyl KetoneHCID 6569—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물2-[(3,4-Dichlorophenyl)dimethylaminomethyl]-1-phenethylcyclo-hexanol, hydrochlorideHCID 131723336137.3%

반응 단계

3.0 g (10.0 mmole) of the 2-[(3,4-dichlorophenyl)dimethylaminomethyl]cyclohexanone prepared according to Example 39 were dissolved in 10 ml of tetrahydrofuran, added dropwise while cooling in an ice bath to 12.0 ml (12.0 mmole) of phenethylmagnesium chloride (1 M solution in tetrahydrofuran) and stirred for 15 hours at RT. The reaction solution was worked up by adding 15 ml of saturated ammonium chloride solution while cooling in an ice bath, and was extracted three times at RT with in each case 15 ml of ether. The combined organic extracts were dried over sodium sulfate, filtered and concentrated by evaporation on a rotary evaporator (500 to 10 mbar). 3.88 g of crude base (95.5% of theory) were obtained from which, after adding 30 ml of n-hexane, an oil was obtained according to the procedure described in Example 1 (3rd Stage) with chlorotrimethylsilane/ water in 2-butanone. After decanting the solvents the oil was stirred in 5 ml of water and 20 ml of ether, arid the resultant precipitate was filtered off and dried. 3.04 g of 2-[(3,4-dichlorophenyl)dimethylaminomethyl]-1-phenethylcyclo-hexanol, hydrochloride (68.7% of theory) were obtained in this way. The hydrochloride decomposes on heating above 130° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06410790B1
출처 데이터셋uspto-grants-2002_06
ORD IDord-b7fe3fad177b43bf8a9cfd81fb5951d7
출처 메모uspto-grants-2002_06