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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968765Generated: October 29, 2026

Water → N-{2-[4(3,4-dichlorophenoxy)-1-piperidinyl]ethyl}-3-methoxybenzamide

https://huagongshe.com/reaction/968765

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactantm-Anisoyl chlorideHCID 74374—
Reactant4-(3,4-Dichlorophenoxy)-1-piperidineethanamineHCID 11358209—
SolventTetrahydrofuranHCID 8028—
ProductN-{2-[4(3,4-dichlorophenoxy)-1-piperidinyl]ethyl}-3-methoxybenzamideHCID 9910169—

Reaction Steps

The product from Example 3, Step b (2.00 g) was dissolved in TBF (100 ml) and triethylamine (2.10 g) added. The solution was then cooled with stirring to 0° C. and to it 3-methoxybenzoyl chloride was added dropwise as a solution in THF (10 ml). Reaction was left to warm to room temp and left for 24 hours then water was added and the organics extracted into ethyl acetate. The combined organics were dried with MgSO4 and the solvent removed by evaporation. The crude product was purified by flash chromatography to leave the sub-title product as a pale yellow oil (1.38 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07304077B2
Source datasetuspto-grants-2007_12
ORD IDord-4ea4457e9599494bbd3bb90bc955551f
Source noteuspto-grants-2007_12