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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1398829Generated: November 3, 2026

Tetrahydrofuran → HCID 86632876, compound

https://huagongshe.com/reaction/1398829

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
Reactant1-Chloro-2,6-dinitrobenzeneHCID 11814—
Reactant5-Aminopentan-1-olHCID 75634—
SolventEthyl AcetateHCID 8857—
ProductHCID 86632876HCID 8663287697%

Reaction Steps

A mixture of 5-amino-1-pentanol (619 mg, 6.00 mmol), 2-chloro-1,3-dinitrobenzene (1.01 g, 4.99 mmol), triethylamine (0.837 mL, 6.01 mmol) and tetrahydrofuran (20 mL) was stirred at room temperature for 1 hr. To the reaction mixture was added 5-amino-1-pentanol (520 mg, 5.04 mmol) at room temperature and the resultant mixture was stirred at room temperature for 0.5 hr. The reaction mixture was diluted with ethyl acetate, washed with water and brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel eluting with a 10-40% ethyl acetate/n-hexane gradient mixture to give the title compound as a yellow oil (1.30 g, 4.82 mmol, 97%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901141B2
Source datasetuspto-grants-2014_12
ORD IDord-08e34a0b4f2445a29e5a9db5c08e0162
Source noteuspto-grants-2014_12