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HRID 36376作成日:2026年10月23日

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

https://huagongshe.com/ja/reaction/36376

反応式

関与物質

役割名称HCID仕込み量
反応物PiperidineHCID 8082—
反応物Captamine HydrochlorideHCID 25798—
反応物Benzyltrimethylammonium hydroxideHCID 66854—
反応物Benzyl 2-BenzylacrylateHCID 10912012—
溶媒MethanolHCID 887—
生成物Phenylmethyl alpha-[[[2-(dimethylamino)ethyl]thio]methyl]benzenepropanoateHCID 1529667124%

反応手順

The title compound of 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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05414018
出典データセットuspto-grants-1995_05
ORD IDord-ec57abf5bbd3413f8d3109fbfd9cb98f
出典メモuspto-grants-1995_05