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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2186315Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/2186315

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 oil prepared in Step 9 (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 chromatography 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
PatentnummerUS06403648B2
Quelldatensatzuspto-grants-2002_06
ORD IDord-38a39fce53664b6394c68d98e2f32edd
Quellennotizuspto-grants-2002_06