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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1018978Generated: October 31, 2026

Sodium Hydroxide → HCID 12972366, compound

https://huagongshe.com/reaction/1018978

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant4-Phenoxybenzoic acidHCID 75182—
ReactantDiphenyl chlorophosphateHCID 75654—
Reactant1-Azabicyclo[2.2.2]octan-3-amine, 2-methyl-, hydrochloride (1:2)HCID 22047063—
SolventTetrahydrofuranHCID 8028—
ProductHCID 12972366HCID 1297236682.7%

Reaction Steps

TEA (0.32 mL, 2.3 mmol, 1 eq) is added to a solution of 4-phenoxybenzoic acid (0.50 g, 2.3 mmol, 1 eq) in 15 mL THF. Diphenylchlorophosphate (0.44 mL, 2.3 mmol, 1 eq) is added and the mixture is stirred at room temperature. After 0.5 h, a suspension of 2-methylquinuclidin-3-amine dihydrochloride from Step N (0.49 g, 2.3 mmol, 1 eq) and TEA (1.30 mL, 9.2 mmol, 4 eq) in THF is added and the resulting mixture is stirred overnight at room temperature. 1N NaOH is added and the aqueous layer is extracted with CHCl3. The combined organic layers are dried over MgSO4, filtered and concentrated to provide 0.64 g (82%) of N-(2-methyl-1-azabicyclo[2.2.2)oct-3-yl)4-phenoxybenzamide. MS (ESI) for C21H24N2O2 m/z 337.3 (M+H)30 . The fumaric acid salt of the product is made and crystallized from IPA to give the product as a white solid. Reverse phase HPLC (ZORBAX Eclipse XDB-C8, 4.6 mm×15 cm, 75:5:20 H2O/CH3CN/IPA) reveals an 85:15 trans/cis mixture of isomers.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06486172B2
Source datasetuspto-grants-2002_11
ORD IDord-9b16a74e9b6b44cd9e7c6e411cf3fdca
Source noteuspto-grants-2002_11