Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Piperidine → Phenylmethyl alpha-[[[2-(dimethylamino)ethyl]thio]methyl]benzenepropanoate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Piperidine | HCID 8082 | — |
| 반응물 | Captamine Hydrochloride | HCID 25798 | — |
| 반응물 | Benzyltrimethylammonium hydroxide | HCID 66854 | — |
| 반응물 | Benzyl 2-Benzylacrylate | HCID 10912012 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | Phenylmethyl alpha-[[[2-(dimethylamino)ethyl]thio]methyl]benzenepropanoate | HCID 15296671 | 24% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05416119 |
| 출처 데이터셋 | uspto-grants-1995_05 |
| ORD ID | ord-41f0d75e5d4744ac88a9dca12e15411d |
| 출처 메모 | uspto-grants-1995_05 |