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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1291164Generated: October 30, 2026

Triethylamine → 1-(3-Nitro-benzyl)-piperidin-4-yl 4-methyl-benzoate

https://huagongshe.com/reaction/1291164

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Methylbenzoyl ChlorideHCID 13405—
ReactantHCID 765448HCID 765448—
SolventTolueneHCID 1140—
Product1-(3-Nitro-benzyl)-piperidin-4-yl 4-methyl-benzoateHCID 1891982973.4%

Reaction Steps

0.65 g (0.00275 mol) of 1-(3-nitro-benzyl)-piperidin-4-ol and 1.9 ml (0.0136 mol) of triethylamine were dissolved in 27.5 ml of toluene, treated with 1.09 ml (0.00825 mol) of 4-methyl-benzoyl chloride and boiled at reflux for 18 hrs. The reaction mixture was concentrated and the residue was chromatographed over silica gel with ethyl acetate/hexane (1:3). 0.715 g (73%) of 1-(3-nitro-benzyl)-piperidin-4-yl 4-methyl-benzoate was obtained as yellow crystals; m.p. 90°-93°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05753679
Source datasetuspto-grants-1998_05
ORD IDord-fd25982ca535471499a005e77956d885
Source noteuspto-grants-1998_05