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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1647536Generated: October 26, 2026

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

https://huagongshe.com/reaction/1647536

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 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05432201
Source datasetuspto-grants-1995_07
ORD IDord-7f03886f3ae14add97200ff807e6ab88
Source noteuspto-grants-1995_07