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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 36747생성일: 2026년 10월 23일

Piperidine → Phenylmethyl alpha-[[[2-(dimethylamino)ethyl]thio]methyl]benzenepropanoate

https://huagongshe.com/ko/reaction/36747

반응식

참여 물질

역할이름HCID투입량
반응물PiperidineHCID 8082—
반응물Captamine HydrochlorideHCID 25798—
반응물Benzyltrimethylammonium hydroxideHCID 66854—
반응물Benzyl 2-BenzylacrylateHCID 10912012—
용매MethanolHCID 887—
생성물Phenylmethyl alpha-[[[2-(dimethylamino)ethyl]thio]methyl]benzenepropanoateHCID 1529667124%

반응 단계

The oil prepared in Step 10 (1.5 g, 5.95 mmol) was dissolved under argon in methanol (22 mL). To this solution was added 2-dimethylaminoethanethiol hydrochloride (843 mg, 5.95 mmol), piperidine (0.78 mL, 7.85 mmol) and benzyltrimethylammonium hydroxide (0.25 mL, 0.6 mmol), and the mixture was stirred at room temperature for 16 hours. The solvent was removed on a rotary evaporator and then the residue was purified by flash chromotography on silica gel, eluting with 20:1 CH2Cl2 :MeOH to give the pure title compound (0.5 g, 24% yield). 1H NMR: 300 MHz spectrum consistent with proposed structure. Anal: calcd. for C21H27NO2S+0.2H2O: C, 69.85; H, 7.65; N, 3.88. Found: C, 69.58; H, 7.60; N, 3.98.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05416119
출처 데이터셋uspto-grants-1995_05
ORD IDord-41f0d75e5d4744ac88a9dca12e15411d
출처 메모uspto-grants-1995_05