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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 378505생성일: 2026년 10월 26일

Diisopropylethylamine → N-[4-(methylcarbonylamino)phenylmethyl]-4-[bis(4-trifluoromethoxyphenyl)hydroxymethyl]piperidine

https://huagongshe.com/reaction/378505

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물Acetamide, N-(4-(chloromethyl)phenyl)-HCID 148705—
반응물4-[Bis(4-trifluoromethoxyphenyl)hydroxymethyl]piperidineHCID 19040926—
용매Dimethyl SulfoxideHCID 679—
생성물N-[4-(methylcarbonylamino)phenylmethyl]-4-[bis(4-trifluoromethoxyphenyl)hydroxymethyl]piperidineHCID 1551518264.4%

반응 단계

To a stirred solution of 0.4 gram (0.0008 mole) of 4-[bis(4-trifluoromethoxyphenyl)hydroxymethyl]piperidine in 10 mL of dimethyl sulfoxide was added a mixture of 0.2 gram (0.0008 mole) of 4-(methylcarbonylamino)phenylmethyl chloride and 0.6 mL (0.003 mole) of N,N-diisopropylethylamine. Upon completion of addition, the reaction mixture was stirred at ambient temperature for about 18 hours. After this time the reaction mixture was partitioned between an aqueous solution saturated with sodium bicarbonate and ethyl acetate. The organic layer was separated and washed with an aqueous solution saturated with sodium chloride. The organic layer was then concentrated under reduced pressure to a residue, which was subjected to column chromatography on silica gel, with methylene chloride and mixtures of 10-50% acetone in methylene chloride as eluants. The product-containing fractions were combined and concentrated under reduced pressure, yielding about 0.3 gram of N-[4-(methylcarbonylamino)phenylmethyl]-4-[bis(4-trifluoromethoxyphenyl)hydroxymethyl]piperidine. The NMR spectrum was consistent with the proposed structure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06030987
출처 데이터셋uspto-grants-2000_02
ORD IDord-3a58e6bb948f417397797c328a2af1ba
출처 메모uspto-grants-2000_02