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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2362522Generated: October 31, 2026

6-Aminohexanoic Acid → Ethyl 6-aminohexanoate hydrochloride

https://huagongshe.com/reaction/2362522

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Aminohexanoic AcidHCID 564—
ReactantTriethylamineHCID 8471—
ReactantThionyl ChlorideHCID 24386—
ReactantEthyl 6-aminohexanoate hydrochlorideHCID 458476—
Reactant4-Chloro-3-nitroquinolineHCID 11275808—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
ProductEthyl 6-aminohexanoate hydrochlorideHCID 458476—
ProductHCID 57447021HCID 57447021—

Reaction Steps

Ethyl 6-aminocaproate hydrochloride was prepared from 6-aminocaproic acid, thionyl chloride, and ethanol by the general method of C. Temple, Jr., R. D. Elliott, and J. A. Montgomery, J. Med. Chem., 1988, 31, 697-700. The general method described in Step 1 of Example 1 was used to react 4-chloro-3-nitroquinoline (41.7 g, 200 mmol), ethyl 6-aminocaproate hydrochloride (46.9 g, 240 mmol) and triethylamine (50.6 g, 500 mmol) in dichloromethane for 15 hours to provide ethyl 6-(3-nitroquinolin-4-ylamino)hexanoate (60.6 g) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691837B2
Source datasetuspto-grants-2014_04
ORD IDord-20b459f5221e49fca7b15eea0820e163
Source noteuspto-grants-2014_04