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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1486027Generated: October 31, 2026

Ethylene Glycol → 6-[[4-(5-carboxypentylcarbamoyl)benzoyl]amino]hexanoic Acid

https://huagongshe.com/reaction/1486027

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantWaterHCID 962—
ReactantSulfuric AcidHCID 1118—
ReactantDimethyl terephthalateHCID 8441—
Reactanthexanoic acid, 6-amino-, monosodium saltHCID 23663648—
Product6-[[4-(5-carboxypentylcarbamoyl)benzoyl]amino]hexanoic AcidHCID 5159834—

Reaction Conditions

Temperature87.5 °C

Reaction Steps

1 equivalent of 6-aminohexanoic acid (ACA), 1 equivalent of sodium hydroxide (NaOH), and suitable amount of water serving as solvent were added into a reaction bottle. After reacting for 2 hours, the reaction bottle was heated to remove the water, and then a solid mixture was obtained. Next, the solid mixture was dried at 90° C. for 12 hours in oven, and then solid 6-aminohexanoic acid sodium salt (ACA-Na) was obtained. Next, 0.97 g (0.005 mole) of dimethyl terephthalate (DMT), 2.32 g (0.015 mole) of dried 6-aminohexanoic acid sodium salt, and 20 ml of ethylene glycol (EG) were put into a reaction bottle. The reaction bottle was heated at 85-90° C. for 14 hours in the presence of nitrogen gas, and then cooled to room temperature and 20 ml of distilled water was added into it. After the solid reactant was dissolved, sulfuric acid aqueous solution (0.1M) was added dropwise slowly into the reaction bottle until the pH value of the solution was 6. Next, after the reaction bottle was set aside at room temperature for 20 hours, a solid precipitate was observed and collected to a glass bottle. Then, the solid precipitate was washed with 3 times weight of distilled water and filtered, and repeated 5 times these washing and filtration steps. Next, the washed solid was dried in an oven at 80° C., N,N′-bis(carboxypentyl)terephthalamide (BCTM) was obtained after drying. The above-mentioned reaction is represented as:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422398B2
Source datasetuspto-grants-2016_08
ORD IDord-a82d963fd68346549cc95ae37089d78f
Source noteuspto-grants-2016_08