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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1291073Generated: October 27, 2026

Triethylamine → 1-Benzyl-piperidin-4-yl 4-nitro-benzoate

https://huagongshe.com/reaction/1291073

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Nitrobenzoyl chlorideHCID 8502—
Reactant1-Benzylpiperidin-4-olHCID 78461—
SolventTolueneHCID 1140—
Product1-Benzyl-piperidin-4-yl 4-nitro-benzoateHCID 18919816106.1%

Reaction Steps

0.5 g (0.00216 mol) of 1-benzyl-4-hydroxypiperidine and 0.64 ml (0.0046 mol) of triethylamine were dissolved in 20 ml of toluene, treated with 0.5 g (0.0027 mol) of 4-nitro-benzoyl chloride and boiled at reflux for 6 hrs. The suspension was filtered, the filtrate was concentrated and the residue was chromatographed over silica gel with ethyl acetatelhexane (1:3) as the eluent. 0.78 g (85%) of 1-benzyl-piperidin-4-yl 4-nitro-benzoate was obtained as yellow crystals; m.p. 87°-89°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05753679
Source datasetuspto-grants-1998_05
ORD IDord-2eb1e9d417994a7ebcba4774e1006ae2
Source noteuspto-grants-1998_05