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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535907Generated: October 30, 2026

Triethylamine → HCID 86687859, compound

https://huagongshe.com/reaction/535907

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-(Chloromethyl)benzoyl chlorideHCID 70136—
Reactant5-Hexyn-1-olHCID 70234—
Reactant4-Amino-1-Boc-piperidineHCID 1268291—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 86687859HCID 86687859—

Reaction Steps

To a solution of 4-(chloromethyl)benzoyl chloride (2.00 g; 10.6 mmol) in THF (30 ml) are added 5-hexyn-1-ol (1.18 ml; 10.6 mmol) and DMAP (0.1 g; 0.82 mmol). The mixture is refluxed overnight with stirring. BOC-4-aminopiperidine (2.33 g; 11.6 mmol) and triethylamine (3.24 ml; 23.3 mmol) are added and the mixture is refluxed for further 3 h. Ethyl acetate (200 ml) and water (50 ml) are added. The organic layer is separated, washed with water and with brine and evaporated to dryness. The residue is purified by silica gel column chromatography (gradient cyclohexane/ethyl acetate 8:2→2:8) to yield 5-Hexyn-1-yl 4-[(4-{[(tertbutoxy)carbonyl]amino}piperidin-1-yl)methyl]-benzoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859559B2
Source datasetuspto-grants-2014_10
ORD IDord-5aa7b02a1c884fe8844357a2db821a01
Source noteuspto-grants-2014_10