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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854199Generated: November 1, 2026

Triethylamine → HCID 86601410, compound

https://huagongshe.com/reaction/854199

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
Reactant4-Nitrophenyl chloroformateHCID 82129—
ReactantHCID 86601408HCID 86601408—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 86601410HCID 8660141085.8%

Reaction Steps

(8E,12E,14E)-3,16,21-tris(1-ethoxyethoxy)-7-hydroxy-6,10,12,16,20-pentamethyl-18,19-epoxytricosa-8,12,14-trien-11-olide (129 mg, 182 μmol) was dissolved in methylene chloride (1 mL). Triethylamine (127 μL, 911 μmol) and 4-dimethylaminopyridine (67.0 mg, 548 μmol) were added to the reaction mixture, and the reaction mixture was stirred at room temperature for 30 minutes. A solution of 4-nitrophenyl chloroformate (112 mg, 556 μmol) in methylene chloride (1 mL) was added dropwise to this reaction mixture and the reaction mixture was stirred at room temperature for 3.5 hours. The reaction mixture was diluted with ethyl acetate (30 mL), and the organic layer was washed with a saturated aqueous solution of sodium hydrogencarbonate (10 mL) and purified water (10 mL) twice, and with brine (10 mL). The resulting organic layer was dried over anhydrous sodium sulfate, filtered and concentrated. The resulting concentrate was purified by silica gel column chromatography (Merck Silica gel 60, 63 to 200 μm; hexane:ethyl acetate=5:1->4:1) to obtain the title compound (137 mg, 156 μmol, 85.8%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07256178B2
Source datasetuspto-grants-2007_08
ORD IDord-004aaaec308146baae11b1b5383f990d
Source noteuspto-grants-2007_08