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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 845328Generated: October 30, 2026

N-Methylpiperidine → HCID 14208556, compound

https://huagongshe.com/reaction/845328

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-MethylpiperidineHCID 12291—
Reactant3-PhenylpropylamineHCID 16259—
ReactantHCID 14208554HCID 14208554—
SolventDichloromethaneHCID 6344—
ProductHCID 14208556HCID 14208556—

Reaction Conditions

Temperature0 °C

Reaction Steps

The title product of Example 2 (7.4 g, 17.9 mmol) dissolved in 75 ml of CH2Cl2 was flushed with Ar and cooled to 0° C. N-methylpiperidine (NMP, 2.2 ml, 17.9 mmol) was added to the reaction before it was cooled to -78° C. and charged with 2.5 ml (17.9 mmol) of IBCF. The reaction was allowed to warm to -15°, maintained at this temperature for 15 min., cooled to -78°, and charged with 2.4 g (17.9 mmol) of 3 phenylpropyl amine (PPA). The crude product, obtained after a reaction work up by the method of Example 1, was chromatographed on a Waters prep 500 using a Porasil cartridge eluting with 2% to 3% ethanol (EtOH)/CH2Cl2. The title product was obtained as a white solid (4.54 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04757153
Source datasetuspto-grants-1988_07
ORD IDord-f5e799514a6844a4826c7a334d3bbbe5
Source noteuspto-grants-1988_07