Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 36376Erstellt: 23. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPiperidineHCID 8082—
EduktCaptamine HydrochlorideHCID 25798—
EduktBenzyltrimethylammonium hydroxideHCID 66854—
EduktBenzyl 2-BenzylacrylateHCID 10912012—
LösungsmittelMethanolHCID 887—
ProduktPhenylmethyl alpha-[[[2-(dimethylamino)ethyl]thio]methyl]benzenepropanoateHCID 1529667124%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05414018
Quelldatensatzuspto-grants-1995_05
ORD IDord-ec57abf5bbd3413f8d3109fbfd9cb98f
Quellennotizuspto-grants-1995_05