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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36747Generated: October 23, 2026

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

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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantCaptamine HydrochlorideHCID 25798—
ReactantBenzyltrimethylammonium hydroxideHCID 66854—
ReactantBenzyl 2-BenzylacrylateHCID 10912012—
SolventMethanolHCID 887—
ProductPhenylmethyl alpha-[[[2-(dimethylamino)ethyl]thio]methyl]benzenepropanoateHCID 1529667124%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05416119
Source datasetuspto-grants-1995_05
ORD IDord-41f0d75e5d4744ac88a9dca12e15411d
Source noteuspto-grants-1995_05