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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1267503Generated: October 25, 2026

Potassium Carbonate → N,N-Diethyl-4-[(8-azabicyclo[3.2.1]oct-3-ylidene)phenylmethyl]benzamide Hydrochloride

https://huagongshe.com/reaction/1267503

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2,2,2-Trichloroethyl chloroformateHCID 87063—
ReactantN,N-diethyl-4-[(8-methyl-8-azabicyclo[3.2.1]oct-3-ylidene)phenylmethyl]benzamideHCID 9952263—
CatalystZincHCID 23994—
SolventBenzeneHCID 241—
ProductN,N-Diethyl-4-[(8-azabicyclo[3.2.1]oct-3-ylidene)phenylmethyl]benzamide HydrochlorideHCID 18545680—

Reaction Steps

A 100 mL benzene suspension of 3.1 g (5.6 mmol) N,N-diethyl-4-[(8-methyl-8-azabicyclo[3.2.1]oct-3-ylidene)phenylmethyl]benzamide, 3.45 g (25 mmol) K2CO3, and 1.5 mL (10 mmol) 2,2,2-trichloroethyl chloroformate was allowed to reflux for 2 h. The reaction was cooled, filtered, and the solvent evaporated. The residual oil was dissolved in MeOH then stirred at reflux with 2.6 g (40 mmol) zinc powder for 1 h. After cooling, the reaction was filtered through celite and partitioned between 3N NaOH and CH2Cl2. The organic layer was washed with brine, dried over K2CO3, filtered, and concentrated (2.1 g, 5.6 mmol). The resulting clear oil was dissolved in Et2O, filtered, and the product precipitated after the addition of ethereal HCl; mp 128-132° C. MS m/z (MH+) 375. 1H NMR 300 MHz (DMSO-d6) δ 7.15-7.4 (m, 9H), 3.9-4.0 (m, 2H), 3.15-3.3 (m, 2H), 2.55-2.65 (m, 2H), 2.25-2.35 (m, 4H), 1.9-2.0 (m, 2H), 1.75-1.85 (m, 2H), 1.0-1.2 (m, 6H). Anal calc C25H30N2O.HCl (3% H2O): C, 70.89; H, 7.71; N, 6.61. Found: C, 70.52; H, 7.41; N, 6.24.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06552036B2
Source datasetuspto-grants-2003_04
ORD IDord-cff11921d3cc40f99a6e17f26982e00d
Source noteuspto-grants-2003_04