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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1489998Generated: October 26, 2026

Triethylamine → HCID 178418646, compound

https://huagongshe.com/reaction/1489998

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTetronic acidHCID 521261—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant6-[4-(Hexyloxy)phenoxy]hexanoic acidHCID 22902790—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
ProductHCID 178418646HCID 17841864643%

Reaction Steps

To a stirring solution of 554 mg (5.54 mmol) of tetronic acid in 20 mL of dimethylformamide is added 850 μL (6.09 mmol) of triethylamine and 220 mg (1.765 mmol) of 4-dimethylaminopyridine at 0° C. Next, 1.26 g (6.63 mmol) of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride and 1.475 g (6.63 mmol) of 6-[4-(hexyloxy)phenoxy]hexanoic acid are added and the reaction mixture is stirred 2 days at room temperature. The reaction is acidified with 1.0N HCI and extracted three times with ether. The combined organic layers are dried over MgSO4 and concentrated in vacuo giving a yellow solid. Pure material is obtained by trituration in ether, filtering to give 774 mg (43%) of 4-hydroxy-3-[6-(4-chlorophenoxy)-1-oxohexyl]-2(5H)-furanone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05679801
Source datasetuspto-grants-1997_10
ORD IDord-df2bc10022bb487ea666d50d500e10ac
Source noteuspto-grants-1997_10